Canonical Allele Identifier: CA381656603

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68846484T>A (hg19) ; chr11:g.69079016T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69079016T>A , CM000673.2:g.69079016T>A	GRCh38
NC_000011.9:g.68846484T>A , CM000673.1:g.68846484T>A	GRCh37
NC_000011.8:g.68603060T>A	NCBI36
NG_016153.1:g.35135T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.392T>A	ENSP00000509200.1:p.Leu131Gln
ENST00000294309.8:c.1535T>A MANE Select	ENSP00000294309.3:p.Leu512Gln
ENST00000635811.1:c.1535T>A	ENSP00000490341.1:p.Leu512Gln
ENST00000637084.1:c.392T>A	ENSP00000490615.1:p.Leu131Gln
ENST00000637342.1:c.1535T>A	ENSP00000490171.1:p.Leu512Gln
ENST00000637504.1:c.1535T>A	ENSP00000489759.1:p.Leu512Gln
ENST00000294309.7:c.1535T>A	ENSP00000294309.3:p.Leu512Gln
ENST00000442692.2:n.1128T>A
ENST00000535009.5:n.1344T>A
ENST00000542467.1:c.1535T>A	ENSP00000445551.1:p.Leu512Gln
NM_139075.3:c.1535T>A	NP_620714.2:p.Leu512Gln
XM_005273824.2:c.1532T>A	XP_005273881.1:p.Leu511Gln
XM_005273826.2:c.1280T>A	XP_005273883.1:p.Leu427Gln
XM_005273827.2:c.1535T>A	XP_005273884.1:p.Leu512Gln
XM_005273828.2:c.1535T>A	XP_005273885.1:p.Leu512Gln
XM_005273830.2:c.842T>A	XP_005273887.1:p.Leu281Gln
XM_005273831.2:c.842T>A	XP_005273888.1:p.Leu281Gln
XM_005273832.2:c.812T>A	XP_005273889.1:p.Leu271Gln
XM_006718453.2:c.1535T>A	XP_006718516.1:p.Leu512Gln
XM_006718454.2:c.1535T>A	XP_006718517.1:p.Leu512Gln
XM_006718456.2:c.1535T>A	XP_006718519.1:p.Leu512Gln
XM_011544802.1:c.1295T>A	XP_011543104.1:p.Leu432Gln
XM_011544803.1:c.1535T>A	XP_011543105.1:p.Leu512Gln
XM_011544804.1:c.1535T>A	XP_011543106.1:p.Leu512Gln
XM_011544805.1:c.1535T>A	XP_011543107.1:p.Leu512Gln
XM_011544806.1:c.1535T>A	XP_011543108.1:p.Leu512Gln
XM_011544807.1:c.839T>A	XP_011543109.1:p.Leu280Gln
XM_011544808.1:c.704T>A	XP_011543110.1:p.Leu235Gln
XR_247191.1:n.1636T>A
XM_005273824.4:c.1532T>A	XP_005273881.1:p.Leu511Gln
XM_005273826.4:c.1280T>A	XP_005273883.1:p.Leu427Gln
XM_005273830.4:c.842T>A	XP_005273887.1:p.Leu281Gln
XM_005273831.4:c.842T>A	XP_005273888.1:p.Leu281Gln
XM_005273832.4:c.812T>A	XP_005273889.1:p.Leu271Gln
XM_011544802.3:c.1295T>A	XP_011543104.1:p.Leu432Gln
XM_011544807.3:c.839T>A	XP_011543109.1:p.Leu280Gln
XM_011544808.3:c.704T>A	XP_011543110.1:p.Leu235Gln
XM_017017328.2:c.1366T>A	XP_016872817.1:p.Cys456Ser
XM_017017329.2:c.1363T>A	XP_016872818.1:p.Cys455Ser
XM_017017330.2:c.812T>A	XP_016872819.1:p.Leu271Gln
XM_017017331.2:c.812T>A	XP_016872820.1:p.Leu271Gln
XM_017017332.2:c.626T>A	XP_016872821.1:p.Leu209Gln
XM_017017333.2:c.643T>A	XP_016872822.1:p.Cys215Ser
XM_017017334.2:c.643T>A	XP_016872823.1:p.Cys215Ser
XM_017017335.2:c.643T>A	XP_016872824.1:p.Cys215Ser
XM_017017336.2:c.535T>A	XP_016872825.1:p.Cys179Ser
XM_024448392.1:c.1325T>A	XP_024304160.1:p.Leu442Gln
XM_024448393.1:c.812T>A	XP_024304161.1:p.Leu271Gln
XR_001747789.2:n.1467T>A
XR_001747790.2:n.1467T>A
XR_247191.3:n.1639T>A
NM_139075.4:c.1535T>A MANE Select	NP_620714.2:p.Leu512Gln