Canonical Allele Identifier: CA428618192

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183680G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426104G>A , CM000664.2:g.127426104G>A	GRCh38
NC_000002.11:g.128183680G>A , CM000664.1:g.128183680G>A	GRCh37
NC_000002.10:g.127900150G>A	NCBI36
NG_016323.1:g.12685G>A , LRG_599:g.12685G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.555G>A MANE Select	ENSP00000234071.4:p.Arg185=
ENST00000234071.7:c.555G>A	ENSP00000234071.3:p.Arg185=
ENST00000402125.2:c.121-2253G>A
ENST00000409048.1:c.657G>A	ENSP00000386679.1:p.Arg219=
ENST00000442644.5:c.498G>A	ENSP00000411241.1:p.Arg166=
ENST00000464089.1:n.141G>A
NM_000312.3:c.555G>A , LRG_599t1:c.555G>A	NP_000303.1:p.Arg185=
XM_005263715.3:c.738G>A	XP_005263772.1:p.Arg246=
XM_005263716.3:c.720G>A	XP_005263773.1:p.Arg240=
XM_005263717.3:c.618G>A	XP_005263774.1:p.Arg206=
XM_005263717.4:c.618G>A	XP_005263774.1:p.Arg206=
XM_017004505.1:c.798G>A	XP_016859994.1:p.Arg266=
XM_024453002.1:c.900G>A	XP_024308770.1:p.Arg300=
XM_024453003.1:c.840G>A	XP_024308771.1:p.Arg280=
XM_024453004.1:c.738G>A	XP_024308772.1:p.Arg246=
XM_024453005.1:c.720G>A	XP_024308773.1:p.Arg240=
XM_024453006.1:c.657G>A	XP_024308774.1:p.Arg219=
XR_923313.2:n.4481C>T
NM_000312.4:c.555G>A MANE Select	NP_000303.1:p.Arg185=
NM_001375602.1:c.738G>A	NP_001362531.1:p.Arg246=
NM_001375603.1:c.720G>A	NP_001362532.1:p.Arg240=
NM_001375604.1:c.618G>A	NP_001362533.1:p.Arg206=
NM_001375605.1:c.657G>A	NP_001362534.1:p.Arg219=
NM_001375606.1:c.723G>A	NP_001362535.1:p.Arg241=
NM_001375607.1:c.741G>A	NP_001362536.1:p.Arg247=
NM_001375608.1:c.498G>A	NP_001362537.1:p.Arg166=
NM_001375609.1:c.531G>A	NP_001362538.1:p.Arg177=
NM_001375610.1:c.549G>A	NP_001362539.1:p.Arg183=
NM_001375611.1:c.555G>A	NP_001362540.1:p.Arg185=
NM_001375613.1:c.555G>A	NP_001362542.1:p.Arg185=