Canonical Allele Identifier: CA1286881934

Gene: PROC

Linked Data

• dbSNP Id: rs1688204474

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127422978G>T , CM000664.2:g.127422978G>T	GRCh38
NC_000002.11:g.128180554G>T , CM000664.1:g.128180554G>T	GRCh37
NC_000002.10:g.127897024G>T	NCBI36
NG_016323.1:g.9559G>T , LRG_599:g.9559G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.262+37G>T MANE Select	ENSP00000234071.4:n.262+37G>T
ENST00000234071.7:c.262+37G>T	ENSP00000234071.3:n.262+37G>T
ENST00000409048.1:c.262+37G>T	ENSP00000386679.1:n.262+37G>T
ENST00000419985.5:c.*68+37G>T	ENSP00000392606.1:n.*68+37G>T
ENST00000427769.5:c.262+37G>T	ENSP00000406295.1:n.262+37G>T
ENST00000429925.5:c.262+37G>T	ENSP00000412697.1:n.262+37G>T
ENST00000431364.1:c.*68+37G>T	ENSP00000391220.1:n.*68+37G>T
ENST00000442644.5:c.262+37G>T	ENSP00000411241.1:n.262+37G>T
ENST00000474030.5:n.382G>T
NM_000312.3:c.262+37G>T , LRG_599t1:c.262+37G>T	NP_000303.1:n.262+37G>T
XM_005263715.3:c.445+37G>T	XP_005263772.1:n.445+37G>T
XM_005263716.3:c.325+37G>T	XP_005263773.1:n.325+37G>T
XM_005263717.3:c.325+37G>T	XP_005263774.1:n.325+37G>T
XM_005263717.4:c.325+37G>T	XP_005263774.1:n.325+37G>T
XM_017004505.1:c.505+37G>T	XP_016859994.1:n.505+37G>T
XM_024453002.1:c.505+37G>T	XP_024308770.1:n.505+37G>T
XM_024453003.1:c.445+37G>T	XP_024308771.1:n.445+37G>T
XM_024453004.1:c.445+37G>T	XP_024308772.1:n.445+37G>T
XM_024453005.1:c.325+37G>T	XP_024308773.1:n.325+37G>T
XM_024453006.1:c.262+37G>T	XP_024308774.1:n.262+37G>T
NM_000312.4:c.262+37G>T MANE Select	NP_000303.1:n.262+37G>T
NM_001375602.1:c.445+37G>T	NP_001362531.1:n.445+37G>T
NM_001375603.1:c.325+37G>T	NP_001362532.1:n.325+37G>T
NM_001375604.1:c.325+37G>T	NP_001362533.1:n.325+37G>T
NM_001375605.1:c.262+37G>T	NP_001362534.1:n.262+37G>T
NM_001375606.1:c.362G>T	NP_001362535.1:p.Arg121Leu
NM_001375607.1:c.346+37G>T	NP_001362536.1:n.346+37G>T
NM_001375608.1:c.262+37G>T	NP_001362537.1:n.262+37G>T
NM_001375609.1:c.238+37G>T	NP_001362538.1:n.238+37G>T
NM_001375610.1:c.256+37G>T	NP_001362539.1:n.256+37G>T
NM_001375611.1:c.262+37G>T	NP_001362540.1:n.262+37G>T
NM_001375613.1:c.262+37G>T	NP_001362542.1:n.262+37G>T