Canonical Allele Identifier: CA4097913

Gene: TCP10L3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167376622C>T , CM000668.2:g.167376622C>T	GRCh38
NC_000006.11:g.167790110C>T , CM000668.1:g.167790110C>T	GRCh37
NC_000006.10:g.167710100C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001366311.1:c.518G>A	NP_001353240.1:p.Arg173His
NM_001366312.1:c.80G>A	NP_001353241.1:p.Arg27His
NM_001366313.1:c.80G>A	NP_001353242.1:p.Arg27His
NM_001366317.1:c.581G>A	NP_001353246.1:p.Arg194His
NM_004610.3:c.500G>A	NP_004601.3:p.Arg167His
NR_163193.1:n.566G>A
NR_163194.1:n.712G>A
NR_163195.1:n.639G>A
NR_163196.1:n.351G>A
ENST00000366827.6:c.500G>A	ENSP00000355792.2:p.Arg167His
ENST00000397829.8:c.500G>A	ENSP00000380929.4:p.Arg167His
ENST00000460930.2:c.488G>A	ENSP00000426065.1:p.Arg163His
ENST00000463894.6:n.1957G>A
ENST00000463894.7:n.1957G>A
ENST00000508373.5:n.1962G>A
ENST00000508373.6:n.1962G>A
ENST00000617120.4:c.578G>A	ENSP00000484621.1:p.Arg193His
ENST00000617120.5:n.325G>A
ENST00000648018.1:n.540-545G>A
ENST00000674952.1:n.540G>A
ENST00000675088.1:n.323G>A
ENST00000675175.1:n.1205G>A
ENST00000675664.1:n.581G>A
XM_011536082.1:c.518G>A	XP_011534384.1:p.Arg173His
XM_011536082.3:c.518G>A	XP_011534384.1:p.Arg173His
XM_011536083.1:c.518G>A	XP_011534385.1:p.Arg173His
XM_011536084.1:c.500G>A	XP_011534386.1:p.Arg167His
XM_011536084.2:c.500G>A	XP_011534386.1:p.Arg167His
XM_011536085.1:c.500G>A	XP_011534387.1:p.Arg167His
XM_011536085.3:c.500G>A	XP_011534387.1:p.Arg167His
XM_011536086.1:c.500G>A	XP_011534388.1:p.Arg167His
XM_011536087.1:c.518G>A	XP_011534389.1:p.Arg173His
XM_011536088.1:c.347G>A	XP_011534390.1:p.Arg116His
XM_011536088.3:c.347G>A	XP_011534390.1:p.Arg116His
XM_011536089.1:c.518G>A	XP_011534391.1:p.Arg173His
XM_011536090.1:c.284G>A	XP_011534392.1:p.Arg95His
XM_011536090.2:c.284G>A	XP_011534392.1:p.Arg95His
XM_011536091.1:c.80G>A	XP_011534393.1:p.Arg27His
XM_011536092.1:c.80G>A	XP_011534394.1:p.Arg27His
XM_017011228.1:c.500G>A	XP_016866717.1:p.Arg167His
XM_017011229.1:c.500G>A	XP_016866718.1:p.Arg167His
XM_017011230.1:c.500G>A	XP_016866719.1:p.Arg167His
XM_017011231.1:c.500G>A	XP_016866720.1:p.Arg167His