Canonical Allele Identifier: CA1859420
Gene: PROC HGNC NCBI

Linked Data

dbSNP Id: rs764436997

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127427067A>G , CM000664.2:g.127427067A>G GRCh38
NC_000002.11:g.128184643A>G , CM000664.1:g.128184643A>G GRCh37
NC_000002.10:g.127901113A>G NCBI36
NG_016323.1:g.13648A>G , LRG_599:g.13648A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.679-38A>G MANE Select ENSP00000234071.4:n.679-38A>G
ENST00000234071.7:c.679-38A>G ENSP00000234071.3:n.679-38A>G
ENST00000402125.2:c.121-1290A>G
ENST00000409048.1:c.781-38A>G ENSP00000386679.1:n.781-38A>G
NM_000312.3:c.679-38A>G , LRG_599t1:c.679-38A>G NP_000303.1:n.679-38A>G
XM_005263715.3:c.862-38A>G XP_005263772.1:n.862-38A>G
XM_005263716.3:c.844-38A>G XP_005263773.1:n.844-38A>G
XM_005263717.3:c.742-38A>G XP_005263774.1:n.742-38A>G
XR_923313.1:n.1486-679T>C
XM_005263717.4:c.742-38A>G XP_005263774.1:n.742-38A>G
XM_017004505.1:c.922-38A>G XP_016859994.1:n.922-38A>G
XM_024453002.1:c.1024-38A>G XP_024308770.1:n.1024-38A>G
XM_024453003.1:c.964-38A>G XP_024308771.1:n.964-38A>G
XM_024453004.1:c.862-38A>G XP_024308772.1:n.862-38A>G
XM_024453005.1:c.844-38A>G XP_024308773.1:n.844-38A>G
XM_024453006.1:c.781-38A>G XP_024308774.1:n.781-38A>G
XR_923313.2:n.4197-679T>C
NM_000312.4:c.679-38A>G MANE Select NP_000303.1:n.679-38A>G
NM_001375602.1:c.862-38A>G NP_001362531.1:n.862-38A>G
NM_001375603.1:c.844-38A>G NP_001362532.1:n.844-38A>G
NM_001375604.1:c.742-38A>G NP_001362533.1:n.742-38A>G
NM_001375605.1:c.781-38A>G NP_001362534.1:n.781-38A>G
NM_001375606.1:c.847-38A>G NP_001362535.1:n.847-38A>G
NM_001375607.1:c.865-38A>G NP_001362536.1:n.865-38A>G
NM_001375608.1:c.622-38A>G NP_001362537.1:n.622-38A>G
NM_001375609.1:c.655-38A>G NP_001362538.1:n.655-38A>G
NM_001375610.1:c.673-38A>G NP_001362539.1:n.673-38A>G
NM_001375611.1:c.679-38A>G NP_001362540.1:n.679-38A>G
NM_001375613.1:c.679-38A>G NP_001362542.1:n.679-38A>G