Canonical Allele Identifier: CA348404891

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186062C>T (hg19) ; chr2:g.127428486C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428486C>T , CM000664.2:g.127428486C>T	GRCh38
NC_000002.11:g.128186062C>T , CM000664.1:g.128186062C>T	GRCh37
NC_000002.10:g.127902532C>T	NCBI36
NG_016323.1:g.15067C>T , LRG_599:g.15067C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.926C>T MANE Select	ENSP00000234071.4:p.Ala309Val
ENST00000234071.7:c.926C>T	ENSP00000234071.3:p.Ala309Val
ENST00000402125.2:c.250C>T
ENST00000409048.1:c.1028C>T	ENSP00000386679.1:p.Ala343Val
NM_000312.3:c.926C>T , LRG_599t1:c.926C>T	NP_000303.1:p.Ala309Val
XM_005263715.3:c.1109C>T	XP_005263772.1:p.Ala370Val
XM_005263716.3:c.1091C>T	XP_005263773.1:p.Ala364Val
XM_005263717.3:c.989C>T	XP_005263774.1:p.Ala330Val
XR_923313.1:n.1332-222G>A
XM_005263717.4:c.989C>T	XP_005263774.1:p.Ala330Val
XM_017004505.1:c.1169C>T	XP_016859994.1:p.Ala390Val
XM_024453002.1:c.1271C>T	XP_024308770.1:p.Ala424Val
XM_024453003.1:c.1211C>T	XP_024308771.1:p.Ala404Val
XM_024453004.1:c.1109C>T	XP_024308772.1:p.Ala370Val
XM_024453005.1:c.1091C>T	XP_024308773.1:p.Ala364Val
XM_024453006.1:c.1028C>T	XP_024308774.1:p.Ala343Val
XR_001739705.1:n.3607-222G>A
XR_923313.2:n.4043-222G>A
NM_000312.4:c.926C>T MANE Select	NP_000303.1:p.Ala309Val
NM_001375602.1:c.1109C>T	NP_001362531.1:p.Ala370Val
NM_001375603.1:c.1091C>T	NP_001362532.1:p.Ala364Val
NM_001375604.1:c.989C>T	NP_001362533.1:p.Ala330Val
NM_001375605.1:c.1028C>T	NP_001362534.1:p.Ala343Val
NM_001375606.1:c.1094C>T	NP_001362535.1:p.Ala365Val
NM_001375607.1:c.1112C>T	NP_001362536.1:p.Ala371Val
NM_001375608.1:c.869C>T	NP_001362537.1:p.Ala290Val
NM_001375609.1:c.902C>T	NP_001362538.1:p.Ala301Val
NM_001375610.1:c.920C>T	NP_001362539.1:p.Ala307Val
NM_001375611.1:c.926C>T	NP_001362540.1:p.Ala309Val
NM_001375613.1:c.926C>T	NP_001362542.1:p.Ala309Val