Canonical Allele Identifier: CA1286884594

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428696A= , CM000664.2:g.127428696A=	GRCh38
NC_000002.11:g.128186272A= , CM000664.1:g.128186272A=	GRCh37
NC_000002.10:g.127902742A=	NCBI36
NG_016323.1:g.15277A= , LRG_599:g.15277A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1136A= MANE Select	ENSP00000234071.4:p.Asn379=
ENST00000234071.7:c.1136A=	ENSP00000234071.3:p.Asn379=
ENST00000402125.2:c.460A=
ENST00000409048.1:c.1238A=	ENSP00000386679.1:p.Asn413=
NM_000312.3:c.1136A= , LRG_599t1:c.1136A=	NP_000303.1:p.Asn379=
XM_005263715.3:c.1319A=	XP_005263772.1:p.Asn440=
XM_005263716.3:c.1301A=	XP_005263773.1:p.Asn434=
XM_005263717.3:c.1199A=	XP_005263774.1:p.Asn400=
XR_923313.1:n.1332-432T=
XM_005263717.4:c.1199A=	XP_005263774.1:p.Asn400=
XM_017004505.1:c.1379A=	XP_016859994.1:p.Asn460=
XM_024453002.1:c.1481A=	XP_024308770.1:p.Asn494=
XM_024453003.1:c.1421A=	XP_024308771.1:p.Asn474=
XM_024453004.1:c.1319A=	XP_024308772.1:p.Asn440=
XM_024453005.1:c.1301A=	XP_024308773.1:p.Asn434=
XM_024453006.1:c.1238A=	XP_024308774.1:p.Asn413=
XR_001739705.1:n.3607-432T=
XR_923313.2:n.4043-432T=
NM_000312.4:c.1136A= MANE Select	NP_000303.1:p.Asn379=
NM_001375602.1:c.1319A=	NP_001362531.1:p.Asn440=
NM_001375603.1:c.1301A=	NP_001362532.1:p.Asn434=
NM_001375604.1:c.1199A=	NP_001362533.1:p.Asn400=
NM_001375605.1:c.1238A=	NP_001362534.1:p.Asn413=
NM_001375606.1:c.1304A=	NP_001362535.1:p.Asn435=
NM_001375607.1:c.1322A=	NP_001362536.1:p.Asn441=
NM_001375608.1:c.1079A=	NP_001362537.1:p.Asn360=
NM_001375609.1:c.1112A=	NP_001362538.1:p.Asn371=
NM_001375610.1:c.1130A=	NP_001362539.1:p.Asn377=
NM_001375611.1:c.1136A=	NP_001362540.1:p.Asn379=
NM_001375613.1:c.1136A=	NP_001362542.1:p.Asn379=