Canonical Allele Identifier: CA348406446

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186386T>C (hg19) ; chr2:g.127428810T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428810T>C , CM000664.2:g.127428810T>C	GRCh38
NC_000002.11:g.128186386T>C , CM000664.1:g.128186386T>C	GRCh37
NC_000002.10:g.127902856T>C	NCBI36
NG_016323.1:g.15391T>C , LRG_599:g.15391T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1250T>C MANE Select	ENSP00000234071.4:p.Val417Ala
ENST00000234071.7:c.1250T>C	ENSP00000234071.3:p.Val417Ala
ENST00000402125.2:c.574T>C
ENST00000409048.1:c.1352T>C	ENSP00000386679.1:p.Val451Ala
NM_000312.3:c.1250T>C , LRG_599t1:c.1250T>C	NP_000303.1:p.Val417Ala
XM_005263715.3:c.1433T>C	XP_005263772.1:p.Val478Ala
XM_005263716.3:c.1415T>C	XP_005263773.1:p.Val472Ala
XM_005263717.3:c.1313T>C	XP_005263774.1:p.Val438Ala
XR_923313.1:n.1332-546A>G
XM_005263717.4:c.1313T>C	XP_005263774.1:p.Val438Ala
XM_017004505.1:c.1493T>C	XP_016859994.1:p.Val498Ala
XM_024453002.1:c.1595T>C	XP_024308770.1:p.Val532Ala
XM_024453003.1:c.1535T>C	XP_024308771.1:p.Val512Ala
XM_024453004.1:c.1433T>C	XP_024308772.1:p.Val478Ala
XM_024453005.1:c.1415T>C	XP_024308773.1:p.Val472Ala
XM_024453006.1:c.1352T>C	XP_024308774.1:p.Val451Ala
XR_001739705.1:n.3607-546A>G
XR_923313.2:n.4043-546A>G
NM_000312.4:c.1250T>C MANE Select	NP_000303.1:p.Val417Ala
NM_001375602.1:c.1433T>C	NP_001362531.1:p.Val478Ala
NM_001375603.1:c.1415T>C	NP_001362532.1:p.Val472Ala
NM_001375604.1:c.1313T>C	NP_001362533.1:p.Val438Ala
NM_001375605.1:c.1352T>C	NP_001362534.1:p.Val451Ala
NM_001375606.1:c.1418T>C	NP_001362535.1:p.Val473Ala
NM_001375607.1:c.1436T>C	NP_001362536.1:p.Val479Ala
NM_001375608.1:c.1193T>C	NP_001362537.1:p.Val398Ala
NM_001375609.1:c.1226T>C	NP_001362538.1:p.Val409Ala
NM_001375610.1:c.1244T>C	NP_001362539.1:p.Val415Ala
NM_001375611.1:c.1250T>C	NP_001362540.1:p.Val417Ala
NM_001375613.1:c.1250T>C	NP_001362542.1:p.Val417Ala