Canonical Allele Identifier: CA348401476
Gene: PROC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426175A>C , CM000664.2:g.127426175A>C GRCh38
NC_000002.11:g.128183751A>C , CM000664.1:g.128183751A>C GRCh37
NC_000002.10:g.127900221A>C NCBI36
NG_016323.1:g.12756A>C , LRG_599:g.12756A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.626A>C MANE Select ENSP00000234071.4:p.Asp209Ala
ENST00000234071.7:c.626A>C ENSP00000234071.3:p.Asp209Ala
ENST00000402125.2:c.121-2182A>C
ENST00000409048.1:c.728A>C ENSP00000386679.1:p.Asp243Ala
ENST00000464089.1:n.212A>C
NM_000312.3:c.626A>C , LRG_599t1:c.626A>C NP_000303.1:p.Asp209Ala
XM_005263715.3:c.809A>C XP_005263772.1:p.Asp270Ala
XM_005263716.3:c.791A>C XP_005263773.1:p.Asp264Ala
XM_005263717.3:c.689A>C XP_005263774.1:p.Asp230Ala
XM_005263717.4:c.689A>C XP_005263774.1:p.Asp230Ala
XM_017004505.1:c.869A>C XP_016859994.1:p.Asp290Ala
XM_024453002.1:c.971A>C XP_024308770.1:p.Asp324Ala
XM_024453003.1:c.911A>C XP_024308771.1:p.Asp304Ala
XM_024453004.1:c.809A>C XP_024308772.1:p.Asp270Ala
XM_024453005.1:c.791A>C XP_024308773.1:p.Asp264Ala
XM_024453006.1:c.728A>C XP_024308774.1:p.Asp243Ala
XR_923313.2:n.4410T>G
NM_000312.4:c.626A>C MANE Select NP_000303.1:p.Asp209Ala
NM_001375602.1:c.809A>C NP_001362531.1:p.Asp270Ala
NM_001375603.1:c.791A>C NP_001362532.1:p.Asp264Ala
NM_001375604.1:c.689A>C NP_001362533.1:p.Asp230Ala
NM_001375605.1:c.728A>C NP_001362534.1:p.Asp243Ala
NM_001375606.1:c.794A>C NP_001362535.1:p.Asp265Ala
NM_001375607.1:c.812A>C NP_001362536.1:p.Asp271Ala
NM_001375608.1:c.569A>C NP_001362537.1:p.Asp190Ala
NM_001375609.1:c.602A>C NP_001362538.1:p.Asp201Ala
NM_001375610.1:c.620A>C NP_001362539.1:p.Asp207Ala
NM_001375611.1:c.626A>C NP_001362540.1:p.Asp209Ala
NM_001375613.1:c.626A>C NP_001362542.1:p.Asp209Ala