Canonical Allele Identifier: CA381656339

Gene: TPCN2

Linked Data

• gnomAD v4: 11-69078955-G-C
• MyVariant Identifiers: chr11:g.68846423G>C (hg19) ; chr11:g.69078955G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078955G>C , CM000673.2:g.69078955G>C	GRCh38
NC_000011.9:g.68846423G>C , CM000673.1:g.68846423G>C	GRCh37
NC_000011.8:g.68602999G>C	NCBI36
NG_016153.1:g.35074G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000692585.1:c.331G>C	ENSP00000509200.1:p.Gly111Arg
ENST00000294309.8:c.1474G>C MANE Select	ENSP00000294309.3:p.Gly492Arg
ENST00000635811.1:c.1474G>C	ENSP00000490341.1:p.Gly492Arg
ENST00000637084.1:c.331G>C	ENSP00000490615.1:p.Gly111Arg
ENST00000637342.1:c.1474G>C	ENSP00000490171.1:p.Gly492Arg
ENST00000637504.1:c.1474G>C	ENSP00000489759.1:p.Gly492Arg
ENST00000294309.7:c.1474G>C	ENSP00000294309.3:p.Gly492Arg
ENST00000442692.2:n.1067G>C
ENST00000535009.5:n.1283G>C
ENST00000542467.1:c.1474G>C	ENSP00000445551.1:p.Gly492Arg
NM_139075.3:c.1474G>C	NP_620714.2:p.Gly492Arg
XM_005273824.2:c.1471G>C	XP_005273881.1:p.Gly491Arg
XM_005273826.2:c.1219G>C	XP_005273883.1:p.Gly407Arg
XM_005273827.2:c.1474G>C	XP_005273884.1:p.Gly492Arg
XM_005273828.2:c.1474G>C	XP_005273885.1:p.Gly492Arg
XM_005273830.2:c.781G>C	XP_005273887.1:p.Gly261Arg
XM_005273831.2:c.781G>C	XP_005273888.1:p.Gly261Arg
XM_005273832.2:c.751G>C	XP_005273889.1:p.Gly251Arg
XM_006718453.2:c.1474G>C	XP_006718516.1:p.Gly492Arg
XM_006718454.2:c.1474G>C	XP_006718517.1:p.Gly492Arg
XM_006718456.2:c.1474G>C	XP_006718519.1:p.Gly492Arg
XM_011544802.1:c.1234G>C	XP_011543104.1:p.Gly412Arg
XM_011544803.1:c.1474G>C	XP_011543105.1:p.Gly492Arg
XM_011544804.1:c.1474G>C	XP_011543106.1:p.Gly492Arg
XM_011544805.1:c.1474G>C	XP_011543107.1:p.Gly492Arg
XM_011544806.1:c.1474G>C	XP_011543108.1:p.Gly492Arg
XM_011544807.1:c.778G>C	XP_011543109.1:p.Gly260Arg
XM_011544808.1:c.643G>C	XP_011543110.1:p.Gly215Arg
XR_247191.1:n.1575G>C
XM_005273824.4:c.1471G>C	XP_005273881.1:p.Gly491Arg
XM_005273826.4:c.1219G>C	XP_005273883.1:p.Gly407Arg
XM_005273830.4:c.781G>C	XP_005273887.1:p.Gly261Arg
XM_005273831.4:c.781G>C	XP_005273888.1:p.Gly261Arg
XM_005273832.4:c.751G>C	XP_005273889.1:p.Gly251Arg
XM_011544802.3:c.1234G>C	XP_011543104.1:p.Gly412Arg
XM_011544807.3:c.778G>C	XP_011543109.1:p.Gly260Arg
XM_011544808.3:c.643G>C	XP_011543110.1:p.Gly215Arg
XM_017017328.2:c.1305G>C	XP_016872817.1:p.Trp435Cys
XM_017017329.2:c.1302G>C	XP_016872818.1:p.Trp434Cys
XM_017017330.2:c.751G>C	XP_016872819.1:p.Gly251Arg
XM_017017331.2:c.751G>C	XP_016872820.1:p.Gly251Arg
XM_017017332.2:c.565G>C	XP_016872821.1:p.Gly189Arg
XM_017017333.2:c.582G>C	XP_016872822.1:p.Trp194Cys
XM_017017334.2:c.582G>C	XP_016872823.1:p.Trp194Cys
XM_017017335.2:c.582G>C	XP_016872824.1:p.Trp194Cys
XM_017017336.2:c.474G>C	XP_016872825.1:p.Trp158Cys
XM_024448392.1:c.1264G>C	XP_024304160.1:p.Gly422Arg
XM_024448393.1:c.751G>C	XP_024304161.1:p.Gly251Arg
XR_001747789.2:n.1406G>C
XR_001747790.2:n.1406G>C
XR_247191.3:n.1578G>C
NM_139075.4:c.1474G>C MANE Select	NP_620714.2:p.Gly492Arg