Canonical Allele Identifier: CA381656292

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68846412T>A (hg19) ; chr11:g.69078944T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078944T>A , CM000673.2:g.69078944T>A	GRCh38
NC_000011.9:g.68846412T>A , CM000673.1:g.68846412T>A	GRCh37
NC_000011.8:g.68602988T>A	NCBI36
NG_016153.1:g.35063T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000692585.1:c.320T>A	ENSP00000509200.1:p.Val107Asp
ENST00000294309.8:c.1463T>A MANE Select	ENSP00000294309.3:p.Val488Asp
ENST00000635811.1:c.1463T>A	ENSP00000490341.1:p.Val488Asp
ENST00000637084.1:c.320T>A	ENSP00000490615.1:p.Val107Asp
ENST00000637342.1:c.1463T>A	ENSP00000490171.1:p.Val488Asp
ENST00000637504.1:c.1463T>A	ENSP00000489759.1:p.Val488Asp
ENST00000294309.7:c.1463T>A	ENSP00000294309.3:p.Val488Asp
ENST00000442692.2:n.1056T>A
ENST00000535009.5:n.1272T>A
ENST00000542467.1:c.1463T>A	ENSP00000445551.1:p.Val488Asp
NM_139075.3:c.1463T>A	NP_620714.2:p.Val488Asp
XM_005273824.2:c.1460T>A	XP_005273881.1:p.Val487Asp
XM_005273826.2:c.1208T>A	XP_005273883.1:p.Val403Asp
XM_005273827.2:c.1463T>A	XP_005273884.1:p.Val488Asp
XM_005273828.2:c.1463T>A	XP_005273885.1:p.Val488Asp
XM_005273830.2:c.770T>A	XP_005273887.1:p.Val257Asp
XM_005273831.2:c.770T>A	XP_005273888.1:p.Val257Asp
XM_005273832.2:c.740T>A	XP_005273889.1:p.Val247Asp
XM_006718453.2:c.1463T>A	XP_006718516.1:p.Val488Asp
XM_006718454.2:c.1463T>A	XP_006718517.1:p.Val488Asp
XM_006718456.2:c.1463T>A	XP_006718519.1:p.Val488Asp
XM_011544802.1:c.1223T>A	XP_011543104.1:p.Val408Asp
XM_011544803.1:c.1463T>A	XP_011543105.1:p.Val488Asp
XM_011544804.1:c.1463T>A	XP_011543106.1:p.Val488Asp
XM_011544805.1:c.1463T>A	XP_011543107.1:p.Val488Asp
XM_011544806.1:c.1463T>A	XP_011543108.1:p.Val488Asp
XM_011544807.1:c.767T>A	XP_011543109.1:p.Val256Asp
XM_011544808.1:c.632T>A	XP_011543110.1:p.Val211Asp
XR_247191.1:n.1564T>A
XM_005273824.4:c.1460T>A	XP_005273881.1:p.Val487Asp
XM_005273826.4:c.1208T>A	XP_005273883.1:p.Val403Asp
XM_005273830.4:c.770T>A	XP_005273887.1:p.Val257Asp
XM_005273831.4:c.770T>A	XP_005273888.1:p.Val257Asp
XM_005273832.4:c.740T>A	XP_005273889.1:p.Val247Asp
XM_011544802.3:c.1223T>A	XP_011543104.1:p.Val408Asp
XM_011544807.3:c.767T>A	XP_011543109.1:p.Val256Asp
XM_011544808.3:c.632T>A	XP_011543110.1:p.Val211Asp
XM_017017328.2:c.1294T>A	XP_016872817.1:p.Ser432Thr
XM_017017329.2:c.1291T>A	XP_016872818.1:p.Ser431Thr
XM_017017330.2:c.740T>A	XP_016872819.1:p.Val247Asp
XM_017017331.2:c.740T>A	XP_016872820.1:p.Val247Asp
XM_017017332.2:c.554T>A	XP_016872821.1:p.Val185Asp
XM_017017333.2:c.571T>A	XP_016872822.1:p.Ser191Thr
XM_017017334.2:c.571T>A	XP_016872823.1:p.Ser191Thr
XM_017017335.2:c.571T>A	XP_016872824.1:p.Ser191Thr
XM_017017336.2:c.463T>A	XP_016872825.1:p.Ser155Thr
XM_024448392.1:c.1253T>A	XP_024304160.1:p.Val418Asp
XM_024448393.1:c.740T>A	XP_024304161.1:p.Val247Asp
XR_001747789.2:n.1395T>A
XR_001747790.2:n.1395T>A
XR_247191.3:n.1567T>A
NM_139075.4:c.1463T>A MANE Select	NP_620714.2:p.Val488Asp