Canonical Allele Identifier: CA428872906

Gene: PROC

Linked Data

• dbSNP Id: rs1415265203
• gnomAD v3: 2-127428613-G-A
• gnomAD v4: 2-127428613-G-A
• MyVariant Identifiers: chr2:g.128186189G>A (hg19) ; chr2:g.127428613G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428613G>A , CM000664.2:g.127428613G>A	GRCh38
NC_000002.11:g.128186189G>A , CM000664.1:g.128186189G>A	GRCh37
NC_000002.10:g.127902659G>A	NCBI36
NG_016323.1:g.15194G>A , LRG_599:g.15194G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1053G>A MANE Select	ENSP00000234071.4:p.Glu351=
ENST00000234071.7:c.1053G>A	ENSP00000234071.3:p.Glu351=
ENST00000402125.2:c.377G>A
ENST00000409048.1:c.1155G>A	ENSP00000386679.1:p.Glu385=
NM_000312.3:c.1053G>A , LRG_599t1:c.1053G>A	NP_000303.1:p.Glu351=
XM_005263715.3:c.1236G>A	XP_005263772.1:p.Glu412=
XM_005263716.3:c.1218G>A	XP_005263773.1:p.Glu406=
XM_005263717.3:c.1116G>A	XP_005263774.1:p.Glu372=
XR_923313.1:n.1332-349C>T
XM_005263717.4:c.1116G>A	XP_005263774.1:p.Glu372=
XM_017004505.1:c.1296G>A	XP_016859994.1:p.Glu432=
XM_024453002.1:c.1398G>A	XP_024308770.1:p.Glu466=
XM_024453003.1:c.1338G>A	XP_024308771.1:p.Glu446=
XM_024453004.1:c.1236G>A	XP_024308772.1:p.Glu412=
XM_024453005.1:c.1218G>A	XP_024308773.1:p.Glu406=
XM_024453006.1:c.1155G>A	XP_024308774.1:p.Glu385=
XR_001739705.1:n.3607-349C>T
XR_923313.2:n.4043-349C>T
NM_000312.4:c.1053G>A MANE Select	NP_000303.1:p.Glu351=
NM_001375602.1:c.1236G>A	NP_001362531.1:p.Glu412=
NM_001375603.1:c.1218G>A	NP_001362532.1:p.Glu406=
NM_001375604.1:c.1116G>A	NP_001362533.1:p.Glu372=
NM_001375605.1:c.1155G>A	NP_001362534.1:p.Glu385=
NM_001375606.1:c.1221G>A	NP_001362535.1:p.Glu407=
NM_001375607.1:c.1239G>A	NP_001362536.1:p.Glu413=
NM_001375608.1:c.996G>A	NP_001362537.1:p.Glu332=
NM_001375609.1:c.1029G>A	NP_001362538.1:p.Glu343=
NM_001375610.1:c.1047G>A	NP_001362539.1:p.Glu349=
NM_001375611.1:c.1053G>A	NP_001362540.1:p.Glu351=
NM_001375613.1:c.1053G>A	NP_001362542.1:p.Glu351=