Canonical Allele Identifier: CA348406084

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186298G>C (hg19) ; chr2:g.127428722G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428722G>C , CM000664.2:g.127428722G>C	GRCh38
NC_000002.11:g.128186298G>C , CM000664.1:g.128186298G>C	GRCh37
NC_000002.10:g.127902768G>C	NCBI36
NG_016323.1:g.15303G>C , LRG_599:g.15303G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1162G>C MANE Select	ENSP00000234071.4:p.Ala388Pro
ENST00000234071.7:c.1162G>C	ENSP00000234071.3:p.Ala388Pro
ENST00000402125.2:c.486G>C
ENST00000409048.1:c.1264G>C	ENSP00000386679.1:p.Ala422Pro
NM_000312.3:c.1162G>C , LRG_599t1:c.1162G>C	NP_000303.1:p.Ala388Pro
XM_005263715.3:c.1345G>C	XP_005263772.1:p.Ala449Pro
XM_005263716.3:c.1327G>C	XP_005263773.1:p.Ala443Pro
XM_005263717.3:c.1225G>C	XP_005263774.1:p.Ala409Pro
XR_923313.1:n.1332-458C>G
XM_005263717.4:c.1225G>C	XP_005263774.1:p.Ala409Pro
XM_017004505.1:c.1405G>C	XP_016859994.1:p.Ala469Pro
XM_024453002.1:c.1507G>C	XP_024308770.1:p.Ala503Pro
XM_024453003.1:c.1447G>C	XP_024308771.1:p.Ala483Pro
XM_024453004.1:c.1345G>C	XP_024308772.1:p.Ala449Pro
XM_024453005.1:c.1327G>C	XP_024308773.1:p.Ala443Pro
XM_024453006.1:c.1264G>C	XP_024308774.1:p.Ala422Pro
XR_001739705.1:n.3607-458C>G
XR_923313.2:n.4043-458C>G
NM_000312.4:c.1162G>C MANE Select	NP_000303.1:p.Ala388Pro
NM_001375602.1:c.1345G>C	NP_001362531.1:p.Ala449Pro
NM_001375603.1:c.1327G>C	NP_001362532.1:p.Ala443Pro
NM_001375604.1:c.1225G>C	NP_001362533.1:p.Ala409Pro
NM_001375605.1:c.1264G>C	NP_001362534.1:p.Ala422Pro
NM_001375606.1:c.1330G>C	NP_001362535.1:p.Ala444Pro
NM_001375607.1:c.1348G>C	NP_001362536.1:p.Ala450Pro
NM_001375608.1:c.1105G>C	NP_001362537.1:p.Ala369Pro
NM_001375609.1:c.1138G>C	NP_001362538.1:p.Ala380Pro
NM_001375610.1:c.1156G>C	NP_001362539.1:p.Ala386Pro
NM_001375611.1:c.1162G>C	NP_001362540.1:p.Ala388Pro
NM_001375613.1:c.1162G>C	NP_001362542.1:p.Ala388Pro