Canonical Allele Identifier: CA1286883464

Gene: PROC

Linked Data

• dbSNP Id: rs1688489414

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426231G>C , CM000664.2:g.127426231G>C	GRCh38
NC_000002.11:g.128183807G>C , CM000664.1:g.128183807G>C	GRCh37
NC_000002.10:g.127900277G>C	NCBI36
NG_016323.1:g.12812G>C , LRG_599:g.12812G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.678+4G>C MANE Select	ENSP00000234071.4:n.678+4G>C
ENST00000234071.7:c.678+4G>C	ENSP00000234071.3:n.678+4G>C
ENST00000402125.2:c.121-2126G>C
ENST00000409048.1:c.780+4G>C	ENSP00000386679.1:n.780+4G>C
ENST00000464089.1:n.268G>C
NM_000312.3:c.678+4G>C , LRG_599t1:c.678+4G>C	NP_000303.1:n.678+4G>C
XM_005263715.3:c.861+4G>C	XP_005263772.1:n.861+4G>C
XM_005263716.3:c.843+4G>C	XP_005263773.1:n.843+4G>C
XM_005263717.3:c.741+4G>C	XP_005263774.1:n.741+4G>C
XM_005263717.4:c.741+4G>C	XP_005263774.1:n.741+4G>C
XM_017004505.1:c.921+4G>C	XP_016859994.1:n.921+4G>C
XM_024453002.1:c.1023+4G>C	XP_024308770.1:n.1023+4G>C
XM_024453003.1:c.963+4G>C	XP_024308771.1:n.963+4G>C
XM_024453004.1:c.861+4G>C	XP_024308772.1:n.861+4G>C
XM_024453005.1:c.843+4G>C	XP_024308773.1:n.843+4G>C
XM_024453006.1:c.780+4G>C	XP_024308774.1:n.780+4G>C
XR_923313.2:n.4354C>G
NM_000312.4:c.678+4G>C MANE Select	NP_000303.1:n.678+4G>C
NM_001375602.1:c.861+4G>C	NP_001362531.1:n.861+4G>C
NM_001375603.1:c.843+4G>C	NP_001362532.1:n.843+4G>C
NM_001375604.1:c.741+4G>C	NP_001362533.1:n.741+4G>C
NM_001375605.1:c.780+4G>C	NP_001362534.1:n.780+4G>C
NM_001375606.1:c.846+4G>C	NP_001362535.1:n.846+4G>C
NM_001375607.1:c.864+4G>C	NP_001362536.1:n.864+4G>C
NM_001375608.1:c.621+4G>C	NP_001362537.1:n.621+4G>C
NM_001375609.1:c.654+4G>C	NP_001362538.1:n.654+4G>C
NM_001375610.1:c.672+4G>C	NP_001362539.1:n.672+4G>C
NM_001375611.1:c.678+4G>C	NP_001362540.1:n.678+4G>C
NM_001375613.1:c.678+4G>C	NP_001362542.1:n.678+4G>C