Canonical Allele Identifier: CA348404477

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128185992T>A (hg19) ; chr2:g.127428416T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428416T>A , CM000664.2:g.127428416T>A	GRCh38
NC_000002.11:g.128185992T>A , CM000664.1:g.128185992T>A	GRCh37
NC_000002.10:g.127902462T>A	NCBI36
NG_016323.1:g.14997T>A , LRG_599:g.14997T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.856T>A MANE Select	ENSP00000234071.4:p.Phe286Ile
ENST00000234071.7:c.856T>A	ENSP00000234071.3:p.Phe286Ile
ENST00000402125.2:c.180T>A
ENST00000409048.1:c.958T>A	ENSP00000386679.1:p.Phe320Ile
NM_000312.3:c.856T>A , LRG_599t1:c.856T>A	NP_000303.1:p.Phe286Ile
XM_005263715.3:c.1039T>A	XP_005263772.1:p.Phe347Ile
XM_005263716.3:c.1021T>A	XP_005263773.1:p.Phe341Ile
XM_005263717.3:c.919T>A	XP_005263774.1:p.Phe307Ile
XR_923313.1:n.1332-152A>T
XM_005263717.4:c.919T>A	XP_005263774.1:p.Phe307Ile
XM_017004505.1:c.1099T>A	XP_016859994.1:p.Phe367Ile
XM_024453002.1:c.1201T>A	XP_024308770.1:p.Phe401Ile
XM_024453003.1:c.1141T>A	XP_024308771.1:p.Phe381Ile
XM_024453004.1:c.1039T>A	XP_024308772.1:p.Phe347Ile
XM_024453005.1:c.1021T>A	XP_024308773.1:p.Phe341Ile
XM_024453006.1:c.958T>A	XP_024308774.1:p.Phe320Ile
XR_001739705.1:n.3607-152A>T
XR_923313.2:n.4043-152A>T
NM_000312.4:c.856T>A MANE Select	NP_000303.1:p.Phe286Ile
NM_001375602.1:c.1039T>A	NP_001362531.1:p.Phe347Ile
NM_001375603.1:c.1021T>A	NP_001362532.1:p.Phe341Ile
NM_001375604.1:c.919T>A	NP_001362533.1:p.Phe307Ile
NM_001375605.1:c.958T>A	NP_001362534.1:p.Phe320Ile
NM_001375606.1:c.1024T>A	NP_001362535.1:p.Phe342Ile
NM_001375607.1:c.1042T>A	NP_001362536.1:p.Phe348Ile
NM_001375608.1:c.799T>A	NP_001362537.1:p.Phe267Ile
NM_001375609.1:c.832T>A	NP_001362538.1:p.Phe278Ile
NM_001375610.1:c.850T>A	NP_001362539.1:p.Phe284Ile
NM_001375611.1:c.856T>A	NP_001362540.1:p.Phe286Ile
NM_001375613.1:c.856T>A	NP_001362542.1:p.Phe286Ile