Canonical Allele Identifier: CA381655986

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68846259G>C (hg19) ; chr11:g.69078791G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69078791G>C , CM000673.2:g.69078791G>C	GRCh38
NC_000011.9:g.68846259G>C , CM000673.1:g.68846259G>C	GRCh37
NC_000011.8:g.68602835G>C	NCBI36
NG_016153.1:g.34910G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692585.1:c.265G>C	ENSP00000509200.1:p.Gly89Arg
ENST00000294309.8:c.1408G>C MANE Select	ENSP00000294309.3:p.Gly470Arg
ENST00000635811.1:c.1408G>C	ENSP00000490341.1:p.Gly470Arg
ENST00000637084.1:c.265G>C	ENSP00000490615.1:p.Gly89Arg
ENST00000637342.1:c.1408G>C	ENSP00000490171.1:p.Gly470Arg
ENST00000637504.1:c.1408G>C	ENSP00000489759.1:p.Gly470Arg
ENST00000294309.7:c.1408G>C	ENSP00000294309.3:p.Gly470Arg
ENST00000442692.2:n.1001G>C
ENST00000535009.5:n.1217G>C
ENST00000542467.1:c.1408G>C	ENSP00000445551.1:p.Gly470Arg
NM_139075.3:c.1408G>C	NP_620714.2:p.Gly470Arg
XM_005273824.2:c.1405G>C	XP_005273881.1:p.Gly469Arg
XM_005273826.2:c.1153G>C	XP_005273883.1:p.Gly385Arg
XM_005273827.2:c.1408G>C	XP_005273884.1:p.Gly470Arg
XM_005273828.2:c.1408G>C	XP_005273885.1:p.Gly470Arg
XM_005273830.2:c.715G>C	XP_005273887.1:p.Gly239Arg
XM_005273831.2:c.715G>C	XP_005273888.1:p.Gly239Arg
XM_005273832.2:c.685G>C	XP_005273889.1:p.Gly229Arg
XM_006718453.2:c.1408G>C	XP_006718516.1:p.Gly470Arg
XM_006718454.2:c.1408G>C	XP_006718517.1:p.Gly470Arg
XM_006718456.2:c.1408G>C	XP_006718519.1:p.Gly470Arg
XM_011544802.1:c.1168G>C	XP_011543104.1:p.Gly390Arg
XM_011544803.1:c.1408G>C	XP_011543105.1:p.Gly470Arg
XM_011544804.1:c.1408G>C	XP_011543106.1:p.Gly470Arg
XM_011544805.1:c.1408G>C	XP_011543107.1:p.Gly470Arg
XM_011544806.1:c.1408G>C	XP_011543108.1:p.Gly470Arg
XM_011544807.1:c.712G>C	XP_011543109.1:p.Gly238Arg
XM_011544808.1:c.577G>C	XP_011543110.1:p.Gly193Arg
XR_247191.1:n.1509G>C
XM_005273824.4:c.1405G>C	XP_005273881.1:p.Gly469Arg
XM_005273826.4:c.1153G>C	XP_005273883.1:p.Gly385Arg
XM_005273830.4:c.715G>C	XP_005273887.1:p.Gly239Arg
XM_005273831.4:c.715G>C	XP_005273888.1:p.Gly239Arg
XM_005273832.4:c.685G>C	XP_005273889.1:p.Gly229Arg
XM_011544802.3:c.1168G>C	XP_011543104.1:p.Gly390Arg
XM_011544807.3:c.712G>C	XP_011543109.1:p.Gly238Arg
XM_011544808.3:c.577G>C	XP_011543110.1:p.Gly193Arg
XM_017017328.2:c.1239G>C	XP_016872817.1:p.Trp413Cys
XM_017017329.2:c.1236G>C	XP_016872818.1:p.Trp412Cys
XM_017017330.2:c.685G>C	XP_016872819.1:p.Gly229Arg
XM_017017331.2:c.685G>C	XP_016872820.1:p.Gly229Arg
XM_017017332.2:c.499G>C	XP_016872821.1:p.Gly167Arg
XM_017017333.2:c.516G>C	XP_016872822.1:p.Trp172Cys
XM_017017334.2:c.516G>C	XP_016872823.1:p.Trp172Cys
XM_017017335.2:c.516G>C	XP_016872824.1:p.Trp172Cys
XM_017017336.2:c.408G>C	XP_016872825.1:p.Trp136Cys
XM_024448392.1:c.1198G>C	XP_024304160.1:p.Gly400Arg
XM_024448393.1:c.685G>C	XP_024304161.1:p.Gly229Arg
XR_001747789.2:n.1340G>C
XR_001747790.2:n.1340G>C
XR_247191.3:n.1512G>C
NM_139075.4:c.1408G>C MANE Select	NP_620714.2:p.Gly470Arg