Canonical Allele Identifier: CA1286883351

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426012A= , CM000664.2:g.127426012A=	GRCh38
NC_000002.11:g.128183588A= , CM000664.1:g.128183588A=	GRCh37
NC_000002.10:g.127900058A=	NCBI36
NG_016323.1:g.12593A= , LRG_599:g.12593A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.536-73A= MANE Select	ENSP00000234071.4:n.536-73A=
ENST00000234071.7:c.536-73A=	ENSP00000234071.3:n.536-73A=
ENST00000402125.2:c.121-2345A=
ENST00000409048.1:c.638-73A=	ENSP00000386679.1:n.638-73A=
ENST00000442644.5:c.479-73A=	ENSP00000411241.1:n.479-73A=
ENST00000464089.1:n.122-73A=
NM_000312.3:c.536-73A= , LRG_599t1:c.536-73A=	NP_000303.1:n.536-73A=
XM_005263715.3:c.719-73A=	XP_005263772.1:n.719-73A=
XM_005263716.3:c.701-73A=	XP_005263773.1:n.701-73A=
XM_005263717.3:c.599-73A=	XP_005263774.1:n.599-73A=
XM_005263717.4:c.599-73A=	XP_005263774.1:n.599-73A=
XM_017004505.1:c.779-73A=	XP_016859994.1:n.779-73A=
XM_024453002.1:c.881-73A=	XP_024308770.1:n.881-73A=
XM_024453003.1:c.821-73A=	XP_024308771.1:n.821-73A=
XM_024453004.1:c.719-73A=	XP_024308772.1:n.719-73A=
XM_024453005.1:c.701-73A=	XP_024308773.1:n.701-73A=
XM_024453006.1:c.638-73A=	XP_024308774.1:n.638-73A=
XR_923313.2:n.4573T=
NM_000312.4:c.536-73A= MANE Select	NP_000303.1:n.536-73A=
NM_001375602.1:c.719-73A=	NP_001362531.1:n.719-73A=
NM_001375603.1:c.701-73A=	NP_001362532.1:n.701-73A=
NM_001375604.1:c.599-73A=	NP_001362533.1:n.599-73A=
NM_001375605.1:c.638-73A=	NP_001362534.1:n.638-73A=
NM_001375606.1:c.704-73A=	NP_001362535.1:n.704-73A=
NM_001375607.1:c.722-73A=	NP_001362536.1:n.722-73A=
NM_001375608.1:c.479-73A=	NP_001362537.1:n.479-73A=
NM_001375609.1:c.512-73A=	NP_001362538.1:n.512-73A=
NM_001375610.1:c.530-73A=	NP_001362539.1:n.530-73A=
NM_001375611.1:c.536-73A=	NP_001362540.1:n.536-73A=
NM_001375613.1:c.536-73A=	NP_001362542.1:n.536-73A=