Canonical Allele Identifier: CA1286884611

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428731C= , CM000664.2:g.127428731C=	GRCh38
NC_000002.11:g.128186307C= , CM000664.1:g.128186307C=	GRCh37
NC_000002.10:g.127902777C=	NCBI36
NG_016323.1:g.15312C= , LRG_599:g.15312C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1171C= MANE Select	ENSP00000234071.4:p.Leu391=
ENST00000234071.7:c.1171C=	ENSP00000234071.3:p.Leu391=
ENST00000402125.2:c.495C=
ENST00000409048.1:c.1273C=	ENSP00000386679.1:p.Leu425=
NM_000312.3:c.1171C= , LRG_599t1:c.1171C=	NP_000303.1:p.Leu391=
XM_005263715.3:c.1354C=	XP_005263772.1:p.Leu452=
XM_005263716.3:c.1336C=	XP_005263773.1:p.Leu446=
XM_005263717.3:c.1234C=	XP_005263774.1:p.Leu412=
XR_923313.1:n.1332-467G=
XM_005263717.4:c.1234C=	XP_005263774.1:p.Leu412=
XM_017004505.1:c.1414C=	XP_016859994.1:p.Leu472=
XM_024453002.1:c.1516C=	XP_024308770.1:p.Leu506=
XM_024453003.1:c.1456C=	XP_024308771.1:p.Leu486=
XM_024453004.1:c.1354C=	XP_024308772.1:p.Leu452=
XM_024453005.1:c.1336C=	XP_024308773.1:p.Leu446=
XM_024453006.1:c.1273C=	XP_024308774.1:p.Leu425=
XR_001739705.1:n.3607-467G=
XR_923313.2:n.4043-467G=
NM_000312.4:c.1171C= MANE Select	NP_000303.1:p.Leu391=
NM_001375602.1:c.1354C=	NP_001362531.1:p.Leu452=
NM_001375603.1:c.1336C=	NP_001362532.1:p.Leu446=
NM_001375604.1:c.1234C=	NP_001362533.1:p.Leu412=
NM_001375605.1:c.1273C=	NP_001362534.1:p.Leu425=
NM_001375606.1:c.1339C=	NP_001362535.1:p.Leu447=
NM_001375607.1:c.1357C=	NP_001362536.1:p.Leu453=
NM_001375608.1:c.1114C=	NP_001362537.1:p.Leu372=
NM_001375609.1:c.1147C=	NP_001362538.1:p.Leu383=
NM_001375610.1:c.1165C=	NP_001362539.1:p.Leu389=
NM_001375611.1:c.1171C=	NP_001362540.1:p.Leu391=
NM_001375613.1:c.1171C=	NP_001362542.1:p.Leu391=