Canonical Allele Identifier: CA1286881994
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127423086C= , CM000664.2:g.127423086C= GRCh38
NC_000002.11:g.128180662C= , CM000664.1:g.128180662C= GRCh37
NC_000002.10:g.127897132C= NCBI36
NG_016323.1:g.9667C= , LRG_599:g.9667C=

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.315C= MANE Select ENSP00000234071.4:p.Cys105=
ENST00000234071.7:c.315C= ENSP00000234071.3:p.Cys105=
ENST00000409048.1:c.315C= ENSP00000386679.1:p.Cys105=
ENST00000419985.5:c.*121C= ENSP00000392606.1:n.*121C=
ENST00000427769.5:c.315C= ENSP00000406295.1:p.Cys105=
ENST00000429925.5:c.315C= ENSP00000412697.1:p.Cys105=
ENST00000431364.1:c.*121C= ENSP00000391220.1:n.*121C=
ENST00000442644.5:c.315C= ENSP00000411241.1:p.Cys105=
ENST00000474030.5:n.490C=
NM_000312.3:c.315C= , LRG_599t1:c.315C= NP_000303.1:p.Cys105=
XM_005263715.3:c.498C= XP_005263772.1:p.Cys166=
XM_005263716.3:c.378C= XP_005263773.1:p.Cys126=
XM_005263717.3:c.378C= XP_005263774.1:p.Cys126=
XM_005263717.4:c.378C= XP_005263774.1:p.Cys126=
XM_017004505.1:c.558C= XP_016859994.1:p.Cys186=
XM_024453002.1:c.558C= XP_024308770.1:p.Cys186=
XM_024453003.1:c.498C= XP_024308771.1:p.Cys166=
XM_024453004.1:c.498C= XP_024308772.1:p.Cys166=
XM_024453005.1:c.378C= XP_024308773.1:p.Cys126=
XM_024453006.1:c.315C= XP_024308774.1:p.Cys105=
NM_000312.4:c.315C= MANE Select NP_000303.1:p.Cys105=
NM_001375602.1:c.498C= NP_001362531.1:p.Cys166=
NM_001375603.1:c.378C= NP_001362532.1:p.Cys126=
NM_001375604.1:c.378C= NP_001362533.1:p.Cys126=
NM_001375605.1:c.315C= NP_001362534.1:p.Cys105=
NM_001375606.1:c.470C= NP_001362535.1:p.Ala157=
NM_001375607.1:c.399C= NP_001362536.1:p.Cys133=
NM_001375608.1:c.315C= NP_001362537.1:p.Cys105=
NM_001375609.1:c.291C= NP_001362538.1:p.Cys97=
NM_001375610.1:c.309C= NP_001362539.1:p.Cys103=
NM_001375611.1:c.315C= NP_001362540.1:p.Cys105=
NM_001375613.1:c.315C= NP_001362542.1:p.Cys105=