Canonical Allele Identifier: CA428873297

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186282T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428706T>A , CM000664.2:g.127428706T>A	GRCh38
NC_000002.11:g.128186282T>A , CM000664.1:g.128186282T>A	GRCh37
NC_000002.10:g.127902752T>A	NCBI36
NG_016323.1:g.15287T>A , LRG_599:g.15287T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1146T>A MANE Select	ENSP00000234071.4:p.Ser382=
ENST00000234071.7:c.1146T>A	ENSP00000234071.3:p.Ser382=
ENST00000402125.2:c.470T>A
ENST00000409048.1:c.1248T>A	ENSP00000386679.1:p.Ser416=
NM_000312.3:c.1146T>A , LRG_599t1:c.1146T>A	NP_000303.1:p.Ser382=
XM_005263715.3:c.1329T>A	XP_005263772.1:p.Ser443=
XM_005263716.3:c.1311T>A	XP_005263773.1:p.Ser437=
XM_005263717.3:c.1209T>A	XP_005263774.1:p.Ser403=
XR_923313.1:n.1332-442A>T
XM_005263717.4:c.1209T>A	XP_005263774.1:p.Ser403=
XM_017004505.1:c.1389T>A	XP_016859994.1:p.Ser463=
XM_024453002.1:c.1491T>A	XP_024308770.1:p.Ser497=
XM_024453003.1:c.1431T>A	XP_024308771.1:p.Ser477=
XM_024453004.1:c.1329T>A	XP_024308772.1:p.Ser443=
XM_024453005.1:c.1311T>A	XP_024308773.1:p.Ser437=
XM_024453006.1:c.1248T>A	XP_024308774.1:p.Ser416=
XR_001739705.1:n.3607-442A>T
XR_923313.2:n.4043-442A>T
NM_000312.4:c.1146T>A MANE Select	NP_000303.1:p.Ser382=
NM_001375602.1:c.1329T>A	NP_001362531.1:p.Ser443=
NM_001375603.1:c.1311T>A	NP_001362532.1:p.Ser437=
NM_001375604.1:c.1209T>A	NP_001362533.1:p.Ser403=
NM_001375605.1:c.1248T>A	NP_001362534.1:p.Ser416=
NM_001375606.1:c.1314T>A	NP_001362535.1:p.Ser438=
NM_001375607.1:c.1332T>A	NP_001362536.1:p.Ser444=
NM_001375608.1:c.1089T>A	NP_001362537.1:p.Ser363=
NM_001375609.1:c.1122T>A	NP_001362538.1:p.Ser374=
NM_001375610.1:c.1140T>A	NP_001362539.1:p.Ser380=
NM_001375611.1:c.1146T>A	NP_001362540.1:p.Ser382=
NM_001375613.1:c.1146T>A	NP_001362542.1:p.Ser382=