Canonical Allele Identifier: CA348406672

Gene: PROC

Linked Data

• dbSNP Id: rs1392922558
• gnomAD v2: 2-128186463-G-A
• gnomAD v3: 2-127428887-G-A
• gnomAD v4: 2-127428887-G-A
• MyVariant Identifiers: chr2:g.128186463G>A (hg19) ; chr2:g.127428887G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428887G>A , CM000664.2:g.127428887G>A	GRCh38
NC_000002.11:g.128186463G>A , CM000664.1:g.128186463G>A	GRCh37
NC_000002.10:g.127902933G>A	NCBI36
NG_016323.1:g.15468G>A , LRG_599:g.15468G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1327G>A MANE Select	ENSP00000234071.4:p.Asp443Asn
ENST00000234071.7:c.1327G>A	ENSP00000234071.3:p.Asp443Asn
ENST00000402125.2:c.651G>A
ENST00000409048.1:c.1429G>A	ENSP00000386679.1:p.Asp477Asn
NM_000312.3:c.1327G>A , LRG_599t1:c.1327G>A	NP_000303.1:p.Asp443Asn
XM_005263715.3:c.1510G>A	XP_005263772.1:p.Asp504Asn
XM_005263716.3:c.1492G>A	XP_005263773.1:p.Asp498Asn
XM_005263717.3:c.1390G>A	XP_005263774.1:p.Asp464Asn
XR_923313.1:n.1332-623C>T
XM_005263717.4:c.1390G>A	XP_005263774.1:p.Asp464Asn
XM_017004505.1:c.1570G>A	XP_016859994.1:p.Asp524Asn
XM_024453002.1:c.1672G>A	XP_024308770.1:p.Asp558Asn
XM_024453003.1:c.1612G>A	XP_024308771.1:p.Asp538Asn
XM_024453004.1:c.1510G>A	XP_024308772.1:p.Asp504Asn
XM_024453005.1:c.1492G>A	XP_024308773.1:p.Asp498Asn
XM_024453006.1:c.1429G>A	XP_024308774.1:p.Asp477Asn
XR_001739705.1:n.3607-623C>T
XR_923313.2:n.4043-623C>T
NM_000312.4:c.1327G>A MANE Select	NP_000303.1:p.Asp443Asn
NM_001375602.1:c.1510G>A	NP_001362531.1:p.Asp504Asn
NM_001375603.1:c.1492G>A	NP_001362532.1:p.Asp498Asn
NM_001375604.1:c.1390G>A	NP_001362533.1:p.Asp464Asn
NM_001375605.1:c.1429G>A	NP_001362534.1:p.Asp477Asn
NM_001375606.1:c.1495G>A	NP_001362535.1:p.Asp499Asn
NM_001375607.1:c.1513G>A	NP_001362536.1:p.Asp505Asn
NM_001375608.1:c.1270G>A	NP_001362537.1:p.Asp424Asn
NM_001375609.1:c.1303G>A	NP_001362538.1:p.Asp435Asn
NM_001375610.1:c.1321G>A	NP_001362539.1:p.Asp441Asn
NM_001375611.1:c.1327G>A	NP_001362540.1:p.Asp443Asn
NM_001375613.1:c.1327G>A	NP_001362542.1:p.Asp443Asn