Canonical Allele Identifier: CA1286881942
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127422991G= , CM000664.2:g.127422991G= GRCh38
NC_000002.11:g.128180567G= , CM000664.1:g.128180567G= GRCh37
NC_000002.10:g.127897037G= NCBI36
NG_016323.1:g.9572G= , LRG_599:g.9572G=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.263-43G= MANE Select ENSP00000234071.4:n.263-43G=
ENST00000234071.7:c.263-43G= ENSP00000234071.3:n.263-43G=
ENST00000409048.1:c.263-43G= ENSP00000386679.1:n.263-43G=
ENST00000419985.5:c.*69-43G= ENSP00000392606.1:n.*69-43G=
ENST00000427769.5:c.263-43G= ENSP00000406295.1:n.263-43G=
ENST00000429925.5:c.263-43G= ENSP00000412697.1:n.263-43G=
ENST00000431364.1:c.*69-43G= ENSP00000391220.1:n.*69-43G=
ENST00000442644.5:c.263-43G= ENSP00000411241.1:n.263-43G=
ENST00000474030.5:n.395G=
NM_000312.3:c.263-43G= , LRG_599t1:c.263-43G= NP_000303.1:n.263-43G=
XM_005263715.3:c.446-43G= XP_005263772.1:n.446-43G=
XM_005263716.3:c.326-43G= XP_005263773.1:n.326-43G=
XM_005263717.3:c.326-43G= XP_005263774.1:n.326-43G=
XM_005263717.4:c.326-43G= XP_005263774.1:n.326-43G=
XM_017004505.1:c.506-43G= XP_016859994.1:n.506-43G=
XM_024453002.1:c.506-43G= XP_024308770.1:n.506-43G=
XM_024453003.1:c.446-43G= XP_024308771.1:n.446-43G=
XM_024453004.1:c.446-43G= XP_024308772.1:n.446-43G=
XM_024453005.1:c.326-43G= XP_024308773.1:n.326-43G=
XM_024453006.1:c.263-43G= XP_024308774.1:n.263-43G=
NM_000312.4:c.263-43G= MANE Select NP_000303.1:n.263-43G=
NM_001375602.1:c.446-43G= NP_001362531.1:n.446-43G=
NM_001375603.1:c.326-43G= NP_001362532.1:n.326-43G=
NM_001375604.1:c.326-43G= NP_001362533.1:n.326-43G=
NM_001375605.1:c.263-43G= NP_001362534.1:n.263-43G=
NM_001375606.1:c.375G= NP_001362535.1:p.Ser125=
NM_001375607.1:c.347-43G= NP_001362536.1:n.347-43G=
NM_001375608.1:c.263-43G= NP_001362537.1:n.263-43G=
NM_001375609.1:c.239-43G= NP_001362538.1:n.239-43G=
NM_001375610.1:c.257-43G= NP_001362539.1:n.257-43G=
NM_001375611.1:c.263-43G= NP_001362540.1:n.263-43G=
NM_001375613.1:c.263-43G= NP_001362542.1:n.263-43G=