Canonical Allele Identifier: CA475209937

Gene: TPCN2

Linked Data

• dbSNP Id: rs1855899589
• MyVariant Identifiers: chr11:g.68846458G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078990G>C , CM000673.2:g.69078990G>C	GRCh38
NC_000011.9:g.68846458G>C , CM000673.1:g.68846458G>C	GRCh37
NC_000011.8:g.68603034G>C	NCBI36
NG_016153.1:g.35109G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.366G>C	ENSP00000509200.1:p.Val122=
ENST00000294309.8:c.1509G>C MANE Select	ENSP00000294309.3:p.Val503=
ENST00000635811.1:c.1509G>C	ENSP00000490341.1:p.Val503=
ENST00000637084.1:c.366G>C	ENSP00000490615.1:p.Val122=
ENST00000637342.1:c.1509G>C	ENSP00000490171.1:p.Val503=
ENST00000637504.1:c.1509G>C	ENSP00000489759.1:p.Val503=
ENST00000294309.7:c.1509G>C	ENSP00000294309.3:p.Val503=
ENST00000442692.2:n.1102G>C
ENST00000535009.5:n.1318G>C
ENST00000542467.1:c.1509G>C	ENSP00000445551.1:p.Val503=
NM_139075.3:c.1509G>C	NP_620714.2:p.Val503=
XM_005273824.2:c.1506G>C	XP_005273881.1:p.Val502=
XM_005273826.2:c.1254G>C	XP_005273883.1:p.Val418=
XM_005273827.2:c.1509G>C	XP_005273884.1:p.Val503=
XM_005273828.2:c.1509G>C	XP_005273885.1:p.Val503=
XM_005273830.2:c.816G>C	XP_005273887.1:p.Val272=
XM_005273831.2:c.816G>C	XP_005273888.1:p.Val272=
XM_005273832.2:c.786G>C	XP_005273889.1:p.Val262=
XM_006718453.2:c.1509G>C	XP_006718516.1:p.Val503=
XM_006718454.2:c.1509G>C	XP_006718517.1:p.Val503=
XM_006718456.2:c.1509G>C	XP_006718519.1:p.Val503=
XM_011544802.1:c.1269G>C	XP_011543104.1:p.Val423=
XM_011544803.1:c.1509G>C	XP_011543105.1:p.Val503=
XM_011544804.1:c.1509G>C	XP_011543106.1:p.Val503=
XM_011544805.1:c.1509G>C	XP_011543107.1:p.Val503=
XM_011544806.1:c.1509G>C	XP_011543108.1:p.Val503=
XM_011544807.1:c.813G>C	XP_011543109.1:p.Val271=
XM_011544808.1:c.678G>C	XP_011543110.1:p.Val226=
XR_247191.1:n.1610G>C
XM_005273824.4:c.1506G>C	XP_005273881.1:p.Val502=
XM_005273826.4:c.1254G>C	XP_005273883.1:p.Val418=
XM_005273830.4:c.816G>C	XP_005273887.1:p.Val272=
XM_005273831.4:c.816G>C	XP_005273888.1:p.Val272=
XM_005273832.4:c.786G>C	XP_005273889.1:p.Val262=
XM_011544802.3:c.1269G>C	XP_011543104.1:p.Val423=
XM_011544807.3:c.813G>C	XP_011543109.1:p.Val271=
XM_011544808.3:c.678G>C	XP_011543110.1:p.Val226=
XM_017017328.2:c.1340G>C	XP_016872817.1:p.Cys447Ser
XM_017017329.2:c.1337G>C	XP_016872818.1:p.Cys446Ser
XM_017017330.2:c.786G>C	XP_016872819.1:p.Val262=
XM_017017331.2:c.786G>C	XP_016872820.1:p.Val262=
XM_017017332.2:c.600G>C	XP_016872821.1:p.Val200=
XM_017017333.2:c.617G>C	XP_016872822.1:p.Cys206Ser
XM_017017334.2:c.617G>C	XP_016872823.1:p.Cys206Ser
XM_017017335.2:c.617G>C	XP_016872824.1:p.Cys206Ser
XM_017017336.2:c.509G>C	XP_016872825.1:p.Cys170Ser
XM_024448392.1:c.1299G>C	XP_024304160.1:p.Val433=
XM_024448393.1:c.786G>C	XP_024304161.1:p.Val262=
XR_001747789.2:n.1441G>C
XR_001747790.2:n.1441G>C
XR_247191.3:n.1613G>C
NM_139075.4:c.1509G>C MANE Select	NP_620714.2:p.Val503=