Canonical Allele Identifier: CA1286883823

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127427066G= , CM000664.2:g.127427066G=	GRCh38
NC_000002.11:g.128184642G= , CM000664.1:g.128184642G=	GRCh37
NC_000002.10:g.127901112G=	NCBI36
NG_016323.1:g.13647G= , LRG_599:g.13647G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.679-39G= MANE Select	ENSP00000234071.4:n.679-39G=
ENST00000234071.7:c.679-39G=	ENSP00000234071.3:n.679-39G=
ENST00000402125.2:c.121-1291G=
ENST00000409048.1:c.781-39G=	ENSP00000386679.1:n.781-39G=
NM_000312.3:c.679-39G= , LRG_599t1:c.679-39G=	NP_000303.1:n.679-39G=
XM_005263715.3:c.862-39G=	XP_005263772.1:n.862-39G=
XM_005263716.3:c.844-39G=	XP_005263773.1:n.844-39G=
XM_005263717.3:c.742-39G=	XP_005263774.1:n.742-39G=
XR_923313.1:n.1486-678C=
XM_005263717.4:c.742-39G=	XP_005263774.1:n.742-39G=
XM_017004505.1:c.922-39G=	XP_016859994.1:n.922-39G=
XM_024453002.1:c.1024-39G=	XP_024308770.1:n.1024-39G=
XM_024453003.1:c.964-39G=	XP_024308771.1:n.964-39G=
XM_024453004.1:c.862-39G=	XP_024308772.1:n.862-39G=
XM_024453005.1:c.844-39G=	XP_024308773.1:n.844-39G=
XM_024453006.1:c.781-39G=	XP_024308774.1:n.781-39G=
XR_923313.2:n.4197-678C=
NM_000312.4:c.679-39G= MANE Select	NP_000303.1:n.679-39G=
NM_001375602.1:c.862-39G=	NP_001362531.1:n.862-39G=
NM_001375603.1:c.844-39G=	NP_001362532.1:n.844-39G=
NM_001375604.1:c.742-39G=	NP_001362533.1:n.742-39G=
NM_001375605.1:c.781-39G=	NP_001362534.1:n.781-39G=
NM_001375606.1:c.847-39G=	NP_001362535.1:n.847-39G=
NM_001375607.1:c.865-39G=	NP_001362536.1:n.865-39G=
NM_001375608.1:c.622-39G=	NP_001362537.1:n.622-39G=
NM_001375609.1:c.655-39G=	NP_001362538.1:n.655-39G=
NM_001375610.1:c.673-39G=	NP_001362539.1:n.673-39G=
NM_001375611.1:c.679-39G=	NP_001362540.1:n.679-39G=
NM_001375613.1:c.679-39G=	NP_001362542.1:n.679-39G=