Canonical Allele Identifier: CA348401704
Gene: PROC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426215C>A , CM000664.2:g.127426215C>A GRCh38
NC_000002.11:g.128183791C>A , CM000664.1:g.128183791C>A GRCh37
NC_000002.10:g.127900261C>A NCBI36
NG_016323.1:g.12796C>A , LRG_599:g.12796C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.666C>A MANE Select ENSP00000234071.4:p.Asp222Glu
ENST00000234071.7:c.666C>A ENSP00000234071.3:p.Asp222Glu
ENST00000402125.2:c.121-2142C>A
ENST00000409048.1:c.768C>A ENSP00000386679.1:p.Asp256Glu
ENST00000464089.1:n.252C>A
NM_000312.3:c.666C>A , LRG_599t1:c.666C>A NP_000303.1:p.Asp222Glu
XM_005263715.3:c.849C>A XP_005263772.1:p.Asp283Glu
XM_005263716.3:c.831C>A XP_005263773.1:p.Asp277Glu
XM_005263717.3:c.729C>A XP_005263774.1:p.Asp243Glu
XM_005263717.4:c.729C>A XP_005263774.1:p.Asp243Glu
XM_017004505.1:c.909C>A XP_016859994.1:p.Asp303Glu
XM_024453002.1:c.1011C>A XP_024308770.1:p.Asp337Glu
XM_024453003.1:c.951C>A XP_024308771.1:p.Asp317Glu
XM_024453004.1:c.849C>A XP_024308772.1:p.Asp283Glu
XM_024453005.1:c.831C>A XP_024308773.1:p.Asp277Glu
XM_024453006.1:c.768C>A XP_024308774.1:p.Asp256Glu
XR_923313.2:n.4370G>T
NM_000312.4:c.666C>A MANE Select NP_000303.1:p.Asp222Glu
NM_001375602.1:c.849C>A NP_001362531.1:p.Asp283Glu
NM_001375603.1:c.831C>A NP_001362532.1:p.Asp277Glu
NM_001375604.1:c.729C>A NP_001362533.1:p.Asp243Glu
NM_001375605.1:c.768C>A NP_001362534.1:p.Asp256Glu
NM_001375606.1:c.834C>A NP_001362535.1:p.Asp278Glu
NM_001375607.1:c.852C>A NP_001362536.1:p.Asp284Glu
NM_001375608.1:c.609C>A NP_001362537.1:p.Asp203Glu
NM_001375609.1:c.642C>A NP_001362538.1:p.Asp214Glu
NM_001375610.1:c.660C>A NP_001362539.1:p.Asp220Glu
NM_001375611.1:c.666C>A NP_001362540.1:p.Asp222Glu
NM_001375613.1:c.666C>A NP_001362542.1:p.Asp222Glu