Canonical Allele Identifier: CA381652154

Gene: TPCN2

Linked Data

• MyVariant Identifiers: chr11:g.68855375T>G (hg19) ; chr11:g.69087907T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.69087907T>G , CM000673.2:g.69087907T>G	GRCh38
NC_000011.9:g.68855375T>G , CM000673.1:g.68855375T>G	GRCh37
NC_000011.8:g.68611951T>G	NCBI36
NG_016153.1:g.44026T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000692585.1:c.1070T>G	ENSP00000509200.1:p.Leu357Arg
ENST00000294309.8:c.2213T>G MANE Select	ENSP00000294309.3:p.Leu738Arg
ENST00000635811.1:c.*408T>G	ENSP00000490341.1:n.*408T>G
ENST00000637084.1:c.1070T>G	ENSP00000490615.1:p.Leu357Arg
ENST00000637342.1:c.2003+1977T>G	ENSP00000490171.1:n.2003+1977T>G
ENST00000637504.1:c.*33+2621T>G	ENSP00000489759.1:n.*33+2621T>G
ENST00000294309.7:c.2213T>G	ENSP00000294309.3:p.Leu738Arg
ENST00000442692.2:n.1679T>G
ENST00000542467.1:c.1667T>G	ENSP00000445551.1:p.Leu556Arg
NM_139075.3:c.2213T>G	NP_620714.2:p.Leu738Arg
XM_005273824.2:c.2210T>G	XP_005273881.1:p.Leu737Arg
XM_005273826.2:c.1958T>G	XP_005273883.1:p.Leu653Arg
XM_005273830.2:c.1520T>G	XP_005273887.1:p.Leu507Arg
XM_005273831.2:c.1520T>G	XP_005273888.1:p.Leu507Arg
XM_005273832.2:c.1490T>G	XP_005273889.1:p.Leu497Arg
XM_006718453.2:c.1639+6408T>G	XP_006718516.1:n.1639+6408T>G
XM_006718454.2:c.1689+6408T>G	XP_006718517.1:n.1689+6408T>G
XM_011544802.1:c.1973T>G	XP_011543104.1:p.Leu658Arg
XM_011544807.1:c.1517T>G	XP_011543109.1:p.Leu506Arg
XM_011544808.1:c.1382T>G	XP_011543110.1:p.Leu461Arg
XR_247191.1:n.2264T>G
XM_005273824.4:c.2210T>G	XP_005273881.1:p.Leu737Arg
XM_005273826.4:c.1958T>G	XP_005273883.1:p.Leu653Arg
XM_005273830.4:c.1520T>G	XP_005273887.1:p.Leu507Arg
XM_005273831.4:c.1520T>G	XP_005273888.1:p.Leu507Arg
XM_005273832.4:c.1490T>G	XP_005273889.1:p.Leu497Arg
XM_011544802.3:c.1973T>G	XP_011543104.1:p.Leu658Arg
XM_011544807.3:c.1517T>G	XP_011543109.1:p.Leu506Arg
XM_011544808.3:c.1382T>G	XP_011543110.1:p.Leu461Arg
XM_017017328.2:c.1994T>G	XP_016872817.1:p.Leu665Arg
XM_017017329.2:c.1991T>G	XP_016872818.1:p.Leu664Arg
XM_017017330.2:c.1490T>G	XP_016872819.1:p.Leu497Arg
XM_017017331.2:c.1490T>G	XP_016872820.1:p.Leu497Arg
XM_017017332.2:c.1304T>G	XP_016872821.1:p.Leu435Arg
XM_017017333.2:c.1271T>G	XP_016872822.1:p.Leu424Arg
XM_017017334.2:c.1271T>G	XP_016872823.1:p.Leu424Arg
XM_017017335.2:c.1271T>G	XP_016872824.1:p.Leu424Arg
XM_017017336.2:c.1163T>G	XP_016872825.1:p.Leu388Arg
XM_024448392.1:c.2003T>G	XP_024304160.1:p.Leu668Arg
XM_024448393.1:c.1490T>G	XP_024304161.1:p.Leu497Arg
XR_001747789.2:n.2145T>G
XR_247191.3:n.2267T>G
NM_139075.4:c.2213T>G MANE Select	NP_620714.2:p.Leu738Arg