Canonical Allele Identifier: CA381656452

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68846452C>A (hg19) ; chr11:g.69078984C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078984C>A , CM000673.2:g.69078984C>A	GRCh38
NC_000011.9:g.68846452C>A , CM000673.1:g.68846452C>A	GRCh37
NC_000011.8:g.68603028C>A	NCBI36
NG_016153.1:g.35103C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.360C>A	ENSP00000509200.1:p.Ser120Arg
ENST00000294309.8:c.1503C>A MANE Select	ENSP00000294309.3:p.Ser501Arg
ENST00000635811.1:c.1503C>A	ENSP00000490341.1:p.Ser501Arg
ENST00000637084.1:c.360C>A	ENSP00000490615.1:p.Ser120Arg
ENST00000637342.1:c.1503C>A	ENSP00000490171.1:p.Ser501Arg
ENST00000637504.1:c.1503C>A	ENSP00000489759.1:p.Ser501Arg
ENST00000294309.7:c.1503C>A	ENSP00000294309.3:p.Ser501Arg
ENST00000442692.2:n.1096C>A
ENST00000535009.5:n.1312C>A
ENST00000542467.1:c.1503C>A	ENSP00000445551.1:p.Ser501Arg
NM_139075.3:c.1503C>A	NP_620714.2:p.Ser501Arg
XM_005273824.2:c.1500C>A	XP_005273881.1:p.Ser500Arg
XM_005273826.2:c.1248C>A	XP_005273883.1:p.Ser416Arg
XM_005273827.2:c.1503C>A	XP_005273884.1:p.Ser501Arg
XM_005273828.2:c.1503C>A	XP_005273885.1:p.Ser501Arg
XM_005273830.2:c.810C>A	XP_005273887.1:p.Ser270Arg
XM_005273831.2:c.810C>A	XP_005273888.1:p.Ser270Arg
XM_005273832.2:c.780C>A	XP_005273889.1:p.Ser260Arg
XM_006718453.2:c.1503C>A	XP_006718516.1:p.Ser501Arg
XM_006718454.2:c.1503C>A	XP_006718517.1:p.Ser501Arg
XM_006718456.2:c.1503C>A	XP_006718519.1:p.Ser501Arg
XM_011544802.1:c.1263C>A	XP_011543104.1:p.Ser421Arg
XM_011544803.1:c.1503C>A	XP_011543105.1:p.Ser501Arg
XM_011544804.1:c.1503C>A	XP_011543106.1:p.Ser501Arg
XM_011544805.1:c.1503C>A	XP_011543107.1:p.Ser501Arg
XM_011544806.1:c.1503C>A	XP_011543108.1:p.Ser501Arg
XM_011544807.1:c.807C>A	XP_011543109.1:p.Ser269Arg
XM_011544808.1:c.672C>A	XP_011543110.1:p.Ser224Arg
XR_247191.1:n.1604C>A
XM_005273824.4:c.1500C>A	XP_005273881.1:p.Ser500Arg
XM_005273826.4:c.1248C>A	XP_005273883.1:p.Ser416Arg
XM_005273830.4:c.810C>A	XP_005273887.1:p.Ser270Arg
XM_005273831.4:c.810C>A	XP_005273888.1:p.Ser270Arg
XM_005273832.4:c.780C>A	XP_005273889.1:p.Ser260Arg
XM_011544802.3:c.1263C>A	XP_011543104.1:p.Ser421Arg
XM_011544807.3:c.807C>A	XP_011543109.1:p.Ser269Arg
XM_011544808.3:c.672C>A	XP_011543110.1:p.Ser224Arg
XM_017017328.2:c.1334C>A	XP_016872817.1:p.Ala445Glu
XM_017017329.2:c.1331C>A	XP_016872818.1:p.Ala444Glu
XM_017017330.2:c.780C>A	XP_016872819.1:p.Ser260Arg
XM_017017331.2:c.780C>A	XP_016872820.1:p.Ser260Arg
XM_017017332.2:c.594C>A	XP_016872821.1:p.Ser198Arg
XM_017017333.2:c.611C>A	XP_016872822.1:p.Ala204Glu
XM_017017334.2:c.611C>A	XP_016872823.1:p.Ala204Glu
XM_017017335.2:c.611C>A	XP_016872824.1:p.Ala204Glu
XM_017017336.2:c.503C>A	XP_016872825.1:p.Ala168Glu
XM_024448392.1:c.1293C>A	XP_024304160.1:p.Ser431Arg
XM_024448393.1:c.780C>A	XP_024304161.1:p.Ser260Arg
XR_001747789.2:n.1435C>A
XR_001747790.2:n.1435C>A
XR_247191.3:n.1607C>A
NM_139075.4:c.1503C>A MANE Select	NP_620714.2:p.Ser501Arg