Canonical Allele Identifier: CA348404771

Gene: PROC

Linked Data

• gnomAD v4: 2-127428468-T-C
• MyVariant Identifiers: chr2:g.128186044T>C (hg19) ; chr2:g.127428468T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428468T>C , CM000664.2:g.127428468T>C	GRCh38
NC_000002.11:g.128186044T>C , CM000664.1:g.128186044T>C	GRCh37
NC_000002.10:g.127902514T>C	NCBI36
NG_016323.1:g.15049T>C , LRG_599:g.15049T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.908T>C MANE Select	ENSP00000234071.4:p.Leu303Pro
ENST00000234071.7:c.908T>C	ENSP00000234071.3:p.Leu303Pro
ENST00000402125.2:c.232T>C
ENST00000409048.1:c.1010T>C	ENSP00000386679.1:p.Leu337Pro
NM_000312.3:c.908T>C , LRG_599t1:c.908T>C	NP_000303.1:p.Leu303Pro
XM_005263715.3:c.1091T>C	XP_005263772.1:p.Leu364Pro
XM_005263716.3:c.1073T>C	XP_005263773.1:p.Leu358Pro
XM_005263717.3:c.971T>C	XP_005263774.1:p.Leu324Pro
XR_923313.1:n.1332-204A>G
XM_005263717.4:c.971T>C	XP_005263774.1:p.Leu324Pro
XM_017004505.1:c.1151T>C	XP_016859994.1:p.Leu384Pro
XM_024453002.1:c.1253T>C	XP_024308770.1:p.Leu418Pro
XM_024453003.1:c.1193T>C	XP_024308771.1:p.Leu398Pro
XM_024453004.1:c.1091T>C	XP_024308772.1:p.Leu364Pro
XM_024453005.1:c.1073T>C	XP_024308773.1:p.Leu358Pro
XM_024453006.1:c.1010T>C	XP_024308774.1:p.Leu337Pro
XR_001739705.1:n.3607-204A>G
XR_923313.2:n.4043-204A>G
NM_000312.4:c.908T>C MANE Select	NP_000303.1:p.Leu303Pro
NM_001375602.1:c.1091T>C	NP_001362531.1:p.Leu364Pro
NM_001375603.1:c.1073T>C	NP_001362532.1:p.Leu358Pro
NM_001375604.1:c.971T>C	NP_001362533.1:p.Leu324Pro
NM_001375605.1:c.1010T>C	NP_001362534.1:p.Leu337Pro
NM_001375606.1:c.1076T>C	NP_001362535.1:p.Leu359Pro
NM_001375607.1:c.1094T>C	NP_001362536.1:p.Leu365Pro
NM_001375608.1:c.851T>C	NP_001362537.1:p.Leu284Pro
NM_001375609.1:c.884T>C	NP_001362538.1:p.Leu295Pro
NM_001375610.1:c.902T>C	NP_001362539.1:p.Leu301Pro
NM_001375611.1:c.908T>C	NP_001362540.1:p.Leu303Pro
NM_001375613.1:c.908T>C	NP_001362542.1:p.Leu303Pro