Canonical Allele Identifier: CA1286884596

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428700G= , CM000664.2:g.127428700G=	GRCh38
NC_000002.11:g.128186276G= , CM000664.1:g.128186276G=	GRCh37
NC_000002.10:g.127902746G=	NCBI36
NG_016323.1:g.15281G= , LRG_599:g.15281G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1140G= MANE Select	ENSP00000234071.4:p.Met380=
ENST00000234071.7:c.1140G=	ENSP00000234071.3:p.Met380=
ENST00000402125.2:c.464G=
ENST00000409048.1:c.1242G=	ENSP00000386679.1:p.Met414=
NM_000312.3:c.1140G= , LRG_599t1:c.1140G=	NP_000303.1:p.Met380=
XM_005263715.3:c.1323G=	XP_005263772.1:p.Met441=
XM_005263716.3:c.1305G=	XP_005263773.1:p.Met435=
XM_005263717.3:c.1203G=	XP_005263774.1:p.Met401=
XR_923313.1:n.1332-436C=
XM_005263717.4:c.1203G=	XP_005263774.1:p.Met401=
XM_017004505.1:c.1383G=	XP_016859994.1:p.Met461=
XM_024453002.1:c.1485G=	XP_024308770.1:p.Met495=
XM_024453003.1:c.1425G=	XP_024308771.1:p.Met475=
XM_024453004.1:c.1323G=	XP_024308772.1:p.Met441=
XM_024453005.1:c.1305G=	XP_024308773.1:p.Met435=
XM_024453006.1:c.1242G=	XP_024308774.1:p.Met414=
XR_001739705.1:n.3607-436C=
XR_923313.2:n.4043-436C=
NM_000312.4:c.1140G= MANE Select	NP_000303.1:p.Met380=
NM_001375602.1:c.1323G=	NP_001362531.1:p.Met441=
NM_001375603.1:c.1305G=	NP_001362532.1:p.Met435=
NM_001375604.1:c.1203G=	NP_001362533.1:p.Met401=
NM_001375605.1:c.1242G=	NP_001362534.1:p.Met414=
NM_001375606.1:c.1308G=	NP_001362535.1:p.Met436=
NM_001375607.1:c.1326G=	NP_001362536.1:p.Met442=
NM_001375608.1:c.1083G=	NP_001362537.1:p.Met361=
NM_001375609.1:c.1116G=	NP_001362538.1:p.Met372=
NM_001375610.1:c.1134G=	NP_001362539.1:p.Met378=
NM_001375611.1:c.1140G=	NP_001362540.1:p.Met380=
NM_001375613.1:c.1140G=	NP_001362542.1:p.Met380=