Canonical Allele Identifier: CA348405805

Gene: PROC

Linked Data

• dbSNP Id: rs1281489645
• gnomAD v2: 2-128186239-T-C
• gnomAD v4: 2-127428663-T-C
• MyVariant Identifiers: chr2:g.128186239T>C (hg19) ; chr2:g.127428663T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428663T>C , CM000664.2:g.127428663T>C	GRCh38
NC_000002.11:g.128186239T>C , CM000664.1:g.128186239T>C	GRCh37
NC_000002.10:g.127902709T>C	NCBI36
NG_016323.1:g.15244T>C , LRG_599:g.15244T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1103T>C MANE Select	ENSP00000234071.4:p.Val368Ala
ENST00000234071.7:c.1103T>C	ENSP00000234071.3:p.Val368Ala
ENST00000402125.2:c.427T>C
ENST00000409048.1:c.1205T>C	ENSP00000386679.1:p.Val402Ala
NM_000312.3:c.1103T>C , LRG_599t1:c.1103T>C	NP_000303.1:p.Val368Ala
XM_005263715.3:c.1286T>C	XP_005263772.1:p.Val429Ala
XM_005263716.3:c.1268T>C	XP_005263773.1:p.Val423Ala
XM_005263717.3:c.1166T>C	XP_005263774.1:p.Val389Ala
XR_923313.1:n.1332-399A>G
XM_005263717.4:c.1166T>C	XP_005263774.1:p.Val389Ala
XM_017004505.1:c.1346T>C	XP_016859994.1:p.Val449Ala
XM_024453002.1:c.1448T>C	XP_024308770.1:p.Val483Ala
XM_024453003.1:c.1388T>C	XP_024308771.1:p.Val463Ala
XM_024453004.1:c.1286T>C	XP_024308772.1:p.Val429Ala
XM_024453005.1:c.1268T>C	XP_024308773.1:p.Val423Ala
XM_024453006.1:c.1205T>C	XP_024308774.1:p.Val402Ala
XR_001739705.1:n.3607-399A>G
XR_923313.2:n.4043-399A>G
NM_000312.4:c.1103T>C MANE Select	NP_000303.1:p.Val368Ala
NM_001375602.1:c.1286T>C	NP_001362531.1:p.Val429Ala
NM_001375603.1:c.1268T>C	NP_001362532.1:p.Val423Ala
NM_001375604.1:c.1166T>C	NP_001362533.1:p.Val389Ala
NM_001375605.1:c.1205T>C	NP_001362534.1:p.Val402Ala
NM_001375606.1:c.1271T>C	NP_001362535.1:p.Val424Ala
NM_001375607.1:c.1289T>C	NP_001362536.1:p.Val430Ala
NM_001375608.1:c.1046T>C	NP_001362537.1:p.Val349Ala
NM_001375609.1:c.1079T>C	NP_001362538.1:p.Val360Ala
NM_001375610.1:c.1097T>C	NP_001362539.1:p.Val366Ala
NM_001375611.1:c.1103T>C	NP_001362540.1:p.Val368Ala
NM_001375613.1:c.1103T>C	NP_001362542.1:p.Val368Ala