Canonical Allele Identifier: CA381656423

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68846445A>C (hg19) ; chr11:g.69078977A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078977A>C , CM000673.2:g.69078977A>C	GRCh38
NC_000011.9:g.68846445A>C , CM000673.1:g.68846445A>C	GRCh37
NC_000011.8:g.68603021A>C	NCBI36
NG_016153.1:g.35096A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.353A>C	ENSP00000509200.1:p.Tyr118Ser
ENST00000294309.8:c.1496A>C MANE Select	ENSP00000294309.3:p.Tyr499Ser
ENST00000635811.1:c.1496A>C	ENSP00000490341.1:p.Tyr499Ser
ENST00000637084.1:c.353A>C	ENSP00000490615.1:p.Tyr118Ser
ENST00000637342.1:c.1496A>C	ENSP00000490171.1:p.Tyr499Ser
ENST00000637504.1:c.1496A>C	ENSP00000489759.1:p.Tyr499Ser
ENST00000294309.7:c.1496A>C	ENSP00000294309.3:p.Tyr499Ser
ENST00000442692.2:n.1089A>C
ENST00000535009.5:n.1305A>C
ENST00000542467.1:c.1496A>C	ENSP00000445551.1:p.Tyr499Ser
NM_139075.3:c.1496A>C	NP_620714.2:p.Tyr499Ser
XM_005273824.2:c.1493A>C	XP_005273881.1:p.Tyr498Ser
XM_005273826.2:c.1241A>C	XP_005273883.1:p.Tyr414Ser
XM_005273827.2:c.1496A>C	XP_005273884.1:p.Tyr499Ser
XM_005273828.2:c.1496A>C	XP_005273885.1:p.Tyr499Ser
XM_005273830.2:c.803A>C	XP_005273887.1:p.Tyr268Ser
XM_005273831.2:c.803A>C	XP_005273888.1:p.Tyr268Ser
XM_005273832.2:c.773A>C	XP_005273889.1:p.Tyr258Ser
XM_006718453.2:c.1496A>C	XP_006718516.1:p.Tyr499Ser
XM_006718454.2:c.1496A>C	XP_006718517.1:p.Tyr499Ser
XM_006718456.2:c.1496A>C	XP_006718519.1:p.Tyr499Ser
XM_011544802.1:c.1256A>C	XP_011543104.1:p.Tyr419Ser
XM_011544803.1:c.1496A>C	XP_011543105.1:p.Tyr499Ser
XM_011544804.1:c.1496A>C	XP_011543106.1:p.Tyr499Ser
XM_011544805.1:c.1496A>C	XP_011543107.1:p.Tyr499Ser
XM_011544806.1:c.1496A>C	XP_011543108.1:p.Tyr499Ser
XM_011544807.1:c.800A>C	XP_011543109.1:p.Tyr267Ser
XM_011544808.1:c.665A>C	XP_011543110.1:p.Tyr222Ser
XR_247191.1:n.1597A>C
XM_005273824.4:c.1493A>C	XP_005273881.1:p.Tyr498Ser
XM_005273826.4:c.1241A>C	XP_005273883.1:p.Tyr414Ser
XM_005273830.4:c.803A>C	XP_005273887.1:p.Tyr268Ser
XM_005273831.4:c.803A>C	XP_005273888.1:p.Tyr268Ser
XM_005273832.4:c.773A>C	XP_005273889.1:p.Tyr258Ser
XM_011544802.3:c.1256A>C	XP_011543104.1:p.Tyr419Ser
XM_011544807.3:c.800A>C	XP_011543109.1:p.Tyr267Ser
XM_011544808.3:c.665A>C	XP_011543110.1:p.Tyr222Ser
XM_017017328.2:c.1327A>C	XP_016872817.1:p.Thr443Pro
XM_017017329.2:c.1324A>C	XP_016872818.1:p.Thr442Pro
XM_017017330.2:c.773A>C	XP_016872819.1:p.Tyr258Ser
XM_017017331.2:c.773A>C	XP_016872820.1:p.Tyr258Ser
XM_017017332.2:c.587A>C	XP_016872821.1:p.Tyr196Ser
XM_017017333.2:c.604A>C	XP_016872822.1:p.Thr202Pro
XM_017017334.2:c.604A>C	XP_016872823.1:p.Thr202Pro
XM_017017335.2:c.604A>C	XP_016872824.1:p.Thr202Pro
XM_017017336.2:c.496A>C	XP_016872825.1:p.Thr166Pro
XM_024448392.1:c.1286A>C	XP_024304160.1:p.Tyr429Ser
XM_024448393.1:c.773A>C	XP_024304161.1:p.Tyr258Ser
XR_001747789.2:n.1428A>C
XR_001747790.2:n.1428A>C
XR_247191.3:n.1600A>C
NM_139075.4:c.1496A>C MANE Select	NP_620714.2:p.Tyr499Ser