Canonical Allele Identifier: CA348406549

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186410G>T (hg19) ; chr2:g.127428834G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428834G>T , CM000664.2:g.127428834G>T	GRCh38
NC_000002.11:g.128186410G>T , CM000664.1:g.128186410G>T	GRCh37
NC_000002.10:g.127902880G>T	NCBI36
NG_016323.1:g.15415G>T , LRG_599:g.15415G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1274G>T MANE Select	ENSP00000234071.4:p.Gly425Val
ENST00000234071.7:c.1274G>T	ENSP00000234071.3:p.Gly425Val
ENST00000402125.2:c.598G>T
ENST00000409048.1:c.1376G>T	ENSP00000386679.1:p.Gly459Val
NM_000312.3:c.1274G>T , LRG_599t1:c.1274G>T	NP_000303.1:p.Gly425Val
XM_005263715.3:c.1457G>T	XP_005263772.1:p.Gly486Val
XM_005263716.3:c.1439G>T	XP_005263773.1:p.Gly480Val
XM_005263717.3:c.1337G>T	XP_005263774.1:p.Gly446Val
XR_923313.1:n.1332-570C>A
XM_005263717.4:c.1337G>T	XP_005263774.1:p.Gly446Val
XM_017004505.1:c.1517G>T	XP_016859994.1:p.Gly506Val
XM_024453002.1:c.1619G>T	XP_024308770.1:p.Gly540Val
XM_024453003.1:c.1559G>T	XP_024308771.1:p.Gly520Val
XM_024453004.1:c.1457G>T	XP_024308772.1:p.Gly486Val
XM_024453005.1:c.1439G>T	XP_024308773.1:p.Gly480Val
XM_024453006.1:c.1376G>T	XP_024308774.1:p.Gly459Val
XR_001739705.1:n.3607-570C>A
XR_923313.2:n.4043-570C>A
NM_000312.4:c.1274G>T MANE Select	NP_000303.1:p.Gly425Val
NM_001375602.1:c.1457G>T	NP_001362531.1:p.Gly486Val
NM_001375603.1:c.1439G>T	NP_001362532.1:p.Gly480Val
NM_001375604.1:c.1337G>T	NP_001362533.1:p.Gly446Val
NM_001375605.1:c.1376G>T	NP_001362534.1:p.Gly459Val
NM_001375606.1:c.1442G>T	NP_001362535.1:p.Gly481Val
NM_001375607.1:c.1460G>T	NP_001362536.1:p.Gly487Val
NM_001375608.1:c.1217G>T	NP_001362537.1:p.Gly406Val
NM_001375609.1:c.1250G>T	NP_001362538.1:p.Gly417Val
NM_001375610.1:c.1268G>T	NP_001362539.1:p.Gly423Val
NM_001375611.1:c.1274G>T	NP_001362540.1:p.Gly425Val
NM_001375613.1:c.1274G>T	NP_001362542.1:p.Gly425Val