Canonical Allele Identifier: CA214354253

Gene: TACC2

Linked Data

• dbSNP Id: rs138805999
• gnomAD v2: 10-123913241-C-T
• gnomAD v3: 10-122153726-C-T
• gnomAD v4: 10-122153726-C-T
• MyVariant Identifiers: chr10:g.123913241C>T (hg19) ; chr10:g.122153726C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122153726C>T , CM000672.2:g.122153726C>T	GRCh38
NC_000010.10:g.123913241C>T , CM000672.1:g.123913241C>T	GRCh37
NC_000010.9:g.123903231C>T	NCBI36
NG_029948.2:g.169553C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369005.6:c.5834+10020C>T MANE Select	ENSP00000358001.1:n.5834+10020C>T
ENST00000334433.7:c.5834+10020C>T	ENSP00000334280.2:n.5834+10020C>T
ENST00000358010.5:c.272+20992C>T	ENSP00000350701.1:n.272+20992C>T
ENST00000369000.5:c.-1055+20992C>T	ENSP00000357996.1:n.-1055+20992C>T
ENST00000369001.5:c.-1151+20992C>T	ENSP00000357997.1:n.-1151+20992C>T
ENST00000369005.5:c.5834+10020C>T	ENSP00000358001.1:n.5834+10020C>T
ENST00000453444.6:c.5846+20992C>T	ENSP00000395048.2:n.5846+20992C>T
ENST00000492237.5:n.174+40497C>T
ENST00000493951.5:n.335+10020C>T
ENST00000513429.5:c.272+20992C>T	ENSP00000425062.1:n.272+20992C>T
ENST00000515273.5:c.5846+20992C>T	ENSP00000424467.1:n.5846+20992C>T
ENST00000515603.5:c.5699+20992C>T	ENSP00000427618.1:n.5699+20992C>T
NM_001291876.1:c.5699+20992C>T	NP_001278805.1:n.5699+20992C>T
NM_001291877.1:c.5846+20992C>T	NP_001278806.1:n.5846+20992C>T
NM_001291879.1:c.-1151+20992C>T	NP_001278808.1:n.-1151+20992C>T
NM_206861.2:c.272+20992C>T	NP_996743.1:n.272+20992C>T
NM_206862.3:c.5834+10020C>T	NP_996744.3:n.5834+10020C>T
XM_005269388.1:c.5894+10020C>T	XP_005269445.1:n.5894+10020C>T
XM_005269389.3:c.5894+10020C>T	XP_005269446.1:n.5894+10020C>T
XM_005269390.1:c.5894+10020C>T	XP_005269447.1:n.5894+10020C>T
XM_005269391.1:c.5834+10020C>T	XP_005269448.1:n.5834+10020C>T
XM_005269392.1:c.5894+10020C>T	XP_005269449.1:n.5894+10020C>T
XM_005269393.1:c.5894+10020C>T	XP_005269450.1:n.5894+10020C>T
XM_005269394.1:c.5768+10020C>T	XP_005269451.1:n.5768+10020C>T
XM_005269395.1:c.5759+20992C>T	XP_005269452.1:n.5759+20992C>T
XM_005269396.1:c.5894+10020C>T	XP_005269453.1:n.5894+10020C>T
XM_005269397.1:c.5634-41314C>T	XP_005269454.1:n.5634-41314C>T
XM_005269399.1:c.5759+20992C>T	XP_005269456.1:n.5759+20992C>T
XM_006717548.1:c.5894+10020C>T	XP_006717611.1:n.5894+10020C>T
XM_006717552.1:c.5894+10020C>T	XP_006717615.1:n.5894+10020C>T
XM_006717553.1:c.5894+10020C>T	XP_006717616.1:n.5894+10020C>T
XM_006717554.1:c.5894+10020C>T	XP_006717617.1:n.5894+10020C>T
XM_011539126.1:c.5891+10020C>T	XP_011537428.1:n.5891+10020C>T
XM_011539127.1:c.5894+10020C>T	XP_011537429.1:n.5894+10020C>T
XM_011539128.1:c.467+10020C>T	XP_011537430.1:n.467+10020C>T
XM_011539129.1:c.332+20992C>T	XP_011537431.1:n.332+20992C>T
XM_011539130.1:c.332+20992C>T	XP_011537432.1:n.332+20992C>T
XM_011539133.1:c.-1055+20992C>T	XP_011537435.1:n.-1055+20992C>T
XM_011539134.1:c.-1055+10020C>T	XP_011537436.1:n.-1055+10020C>T
XM_011539135.1:c.-1055+40493C>T	XP_011537437.1:n.-1055+40493C>T
XM_011539134.2:c.-1055+10020C>T	XP_011537436.1:n.-1055+10020C>T
XM_017015484.1:c.5894+10020C>T	XP_016870973.1:n.5894+10020C>T
XM_017015485.1:c.5894+10020C>T	XP_016870974.1:n.5894+10020C>T
XM_017015486.1:c.5894+10020C>T	XP_016870975.1:n.5894+10020C>T
XM_017015487.1:c.5894+10020C>T	XP_016870976.1:n.5894+10020C>T
XM_017015488.1:c.5634-41314C>T	XP_016870977.1:n.5634-41314C>T
XM_017015489.1:c.5634-41314C>T	XP_016870978.1:n.5634-41314C>T
XM_017015499.1:c.-1055+10020C>T	XP_016870988.1:n.-1055+10020C>T
XM_024447756.1:c.5894+10020C>T	XP_024303524.1:n.5894+10020C>T
XM_024447757.1:c.5894+10020C>T	XP_024303525.1:n.5894+10020C>T
XM_024447758.1:c.5891+10020C>T	XP_024303526.1:n.5891+10020C>T
XM_024447759.1:c.5834+10020C>T	XP_024303527.1:n.5834+10020C>T
XM_024447760.1:c.5768+10020C>T	XP_024303528.1:n.5768+10020C>T
XM_024447761.1:c.5759+20992C>T	XP_024303529.1:n.5759+20992C>T
XM_024447762.1:c.5634-41314C>T	XP_024303530.1:n.5634-41314C>T
XM_024447763.1:c.467+10020C>T	XP_024303531.1:n.467+10020C>T
XM_024447764.1:c.332+20992C>T	XP_024303532.1:n.332+20992C>T
XM_024447766.1:c.-1055+20992C>T	XP_024303534.1:n.-1055+20992C>T
XM_024447767.1:c.-1055+10020C>T	XP_024303535.1:n.-1055+10020C>T
XM_024447768.1:c.-1055+40493C>T	XP_024303536.1:n.-1055+40493C>T
NM_206862.4:c.5834+10020C>T MANE Select	NP_996744.4:n.5834+10020C>T
NM_001291876.2:c.5699+20992C>T	NP_001278805.2:n.5699+20992C>T
NM_001291877.2:c.5846+20992C>T	NP_001278806.2:n.5846+20992C>T
NM_001291879.2:c.-1151+20992C>T	NP_001278808.1:n.-1151+20992C>T
NM_206861.3:c.272+20992C>T	NP_996743.1:n.272+20992C>T