Canonical Allele Identifier: CA1286883467

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426236C= , CM000664.2:g.127426236C=	GRCh38
NC_000002.11:g.128183812C= , CM000664.1:g.128183812C=	GRCh37
NC_000002.10:g.127900282C=	NCBI36
NG_016323.1:g.12817C= , LRG_599:g.12817C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.678+9C= MANE Select	ENSP00000234071.4:n.678+9C=
ENST00000234071.7:c.678+9C=	ENSP00000234071.3:n.678+9C=
ENST00000402125.2:c.121-2121C=
ENST00000409048.1:c.780+9C=	ENSP00000386679.1:n.780+9C=
ENST00000464089.1:n.273C=
NM_000312.3:c.678+9C= , LRG_599t1:c.678+9C=	NP_000303.1:n.678+9C=
XM_005263715.3:c.861+9C=	XP_005263772.1:n.861+9C=
XM_005263716.3:c.843+9C=	XP_005263773.1:n.843+9C=
XM_005263717.3:c.741+9C=	XP_005263774.1:n.741+9C=
XR_923313.1:n.1638G=
XM_005263717.4:c.741+9C=	XP_005263774.1:n.741+9C=
XM_017004505.1:c.921+9C=	XP_016859994.1:n.921+9C=
XM_024453002.1:c.1023+9C=	XP_024308770.1:n.1023+9C=
XM_024453003.1:c.963+9C=	XP_024308771.1:n.963+9C=
XM_024453004.1:c.861+9C=	XP_024308772.1:n.861+9C=
XM_024453005.1:c.843+9C=	XP_024308773.1:n.843+9C=
XM_024453006.1:c.780+9C=	XP_024308774.1:n.780+9C=
XR_923313.2:n.4349G=
NM_000312.4:c.678+9C= MANE Select	NP_000303.1:n.678+9C=
NM_001375602.1:c.861+9C=	NP_001362531.1:n.861+9C=
NM_001375603.1:c.843+9C=	NP_001362532.1:n.843+9C=
NM_001375604.1:c.741+9C=	NP_001362533.1:n.741+9C=
NM_001375605.1:c.780+9C=	NP_001362534.1:n.780+9C=
NM_001375606.1:c.846+9C=	NP_001362535.1:n.846+9C=
NM_001375607.1:c.864+9C=	NP_001362536.1:n.864+9C=
NM_001375608.1:c.621+9C=	NP_001362537.1:n.621+9C=
NM_001375609.1:c.654+9C=	NP_001362538.1:n.654+9C=
NM_001375610.1:c.672+9C=	NP_001362539.1:n.672+9C=
NM_001375611.1:c.678+9C=	NP_001362540.1:n.678+9C=
NM_001375613.1:c.678+9C=	NP_001362542.1:n.678+9C=