Canonical Allele Identifier: CA1286884582

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428673T= , CM000664.2:g.127428673T=	GRCh38
NC_000002.11:g.128186249T= , CM000664.1:g.128186249T=	GRCh37
NC_000002.10:g.127902719T=	NCBI36
NG_016323.1:g.15254T= , LRG_599:g.15254T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1113T= MANE Select	ENSP00000234071.4:p.Asn371=
ENST00000234071.7:c.1113T=	ENSP00000234071.3:p.Asn371=
ENST00000402125.2:c.437T=
ENST00000409048.1:c.1215T=	ENSP00000386679.1:p.Asn405=
NM_000312.3:c.1113T= , LRG_599t1:c.1113T=	NP_000303.1:p.Asn371=
XM_005263715.3:c.1296T=	XP_005263772.1:p.Asn432=
XM_005263716.3:c.1278T=	XP_005263773.1:p.Asn426=
XM_005263717.3:c.1176T=	XP_005263774.1:p.Asn392=
XR_923313.1:n.1332-409A=
XM_005263717.4:c.1176T=	XP_005263774.1:p.Asn392=
XM_017004505.1:c.1356T=	XP_016859994.1:p.Asn452=
XM_024453002.1:c.1458T=	XP_024308770.1:p.Asn486=
XM_024453003.1:c.1398T=	XP_024308771.1:p.Asn466=
XM_024453004.1:c.1296T=	XP_024308772.1:p.Asn432=
XM_024453005.1:c.1278T=	XP_024308773.1:p.Asn426=
XM_024453006.1:c.1215T=	XP_024308774.1:p.Asn405=
XR_001739705.1:n.3607-409A=
XR_923313.2:n.4043-409A=
NM_000312.4:c.1113T= MANE Select	NP_000303.1:p.Asn371=
NM_001375602.1:c.1296T=	NP_001362531.1:p.Asn432=
NM_001375603.1:c.1278T=	NP_001362532.1:p.Asn426=
NM_001375604.1:c.1176T=	NP_001362533.1:p.Asn392=
NM_001375605.1:c.1215T=	NP_001362534.1:p.Asn405=
NM_001375606.1:c.1281T=	NP_001362535.1:p.Asn427=
NM_001375607.1:c.1299T=	NP_001362536.1:p.Asn433=
NM_001375608.1:c.1056T=	NP_001362537.1:p.Asn352=
NM_001375609.1:c.1089T=	NP_001362538.1:p.Asn363=
NM_001375610.1:c.1107T=	NP_001362539.1:p.Asn369=
NM_001375611.1:c.1113T=	NP_001362540.1:p.Asn371=
NM_001375613.1:c.1113T=	NP_001362542.1:p.Asn371=