Canonical Allele Identifier: CA348404879

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428485G>C , CM000664.2:g.127428485G>C	GRCh38
NC_000002.11:g.128186061G>C , CM000664.1:g.128186061G>C	GRCh37
NC_000002.10:g.127902531G>C	NCBI36
NG_016323.1:g.15066G>C , LRG_599:g.15066G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.925G>C MANE Select	ENSP00000234071.4:p.Ala309Pro
ENST00000234071.7:c.925G>C	ENSP00000234071.3:p.Ala309Pro
ENST00000402125.2:c.249G>C
ENST00000409048.1:c.1027G>C	ENSP00000386679.1:p.Ala343Pro
NM_000312.3:c.925G>C , LRG_599t1:c.925G>C	NP_000303.1:p.Ala309Pro
XM_005263715.3:c.1108G>C	XP_005263772.1:p.Ala370Pro
XM_005263716.3:c.1090G>C	XP_005263773.1:p.Ala364Pro
XM_005263717.3:c.988G>C	XP_005263774.1:p.Ala330Pro
XR_923313.1:n.1332-221C>G
XM_005263717.4:c.988G>C	XP_005263774.1:p.Ala330Pro
XM_017004505.1:c.1168G>C	XP_016859994.1:p.Ala390Pro
XM_024453002.1:c.1270G>C	XP_024308770.1:p.Ala424Pro
XM_024453003.1:c.1210G>C	XP_024308771.1:p.Ala404Pro
XM_024453004.1:c.1108G>C	XP_024308772.1:p.Ala370Pro
XM_024453005.1:c.1090G>C	XP_024308773.1:p.Ala364Pro
XM_024453006.1:c.1027G>C	XP_024308774.1:p.Ala343Pro
XR_001739705.1:n.3607-221C>G
XR_923313.2:n.4043-221C>G
NM_000312.4:c.925G>C MANE Select	NP_000303.1:p.Ala309Pro
NM_001375602.1:c.1108G>C	NP_001362531.1:p.Ala370Pro
NM_001375603.1:c.1090G>C	NP_001362532.1:p.Ala364Pro
NM_001375604.1:c.988G>C	NP_001362533.1:p.Ala330Pro
NM_001375605.1:c.1027G>C	NP_001362534.1:p.Ala343Pro
NM_001375606.1:c.1093G>C	NP_001362535.1:p.Ala365Pro
NM_001375607.1:c.1111G>C	NP_001362536.1:p.Ala371Pro
NM_001375608.1:c.868G>C	NP_001362537.1:p.Ala290Pro
NM_001375609.1:c.901G>C	NP_001362538.1:p.Ala301Pro
NM_001375610.1:c.919G>C	NP_001362539.1:p.Ala307Pro
NM_001375611.1:c.925G>C	NP_001362540.1:p.Ala309Pro
NM_001375613.1:c.925G>C	NP_001362542.1:p.Ala309Pro