Canonical Allele Identifier: CA348398086
Gene: PROC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127421403G>A , CM000664.2:g.127421403G>A GRCh38
NC_000002.11:g.128178979G>A , CM000664.1:g.128178979G>A GRCh37
NC_000002.10:g.127895449G>A NCBI36
NG_016323.1:g.7984G>A , LRG_599:g.7984G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.191G>A MANE Select ENSP00000234071.4:p.Cys64Tyr
ENST00000234071.7:c.191G>A ENSP00000234071.3:p.Cys64Tyr
ENST00000409048.1:c.191G>A ENSP00000386679.1:p.Cys64Tyr
ENST00000419985.5:c.156G>A ENSP00000392606.1:p.Leu52=
ENST00000427769.5:c.191G>A ENSP00000406295.1:p.Cys64Tyr
ENST00000429925.5:c.191G>A ENSP00000412697.1:p.Cys64Tyr
ENST00000431364.1:c.156G>A ENSP00000391220.1:p.Leu52=
ENST00000442644.5:c.191G>A ENSP00000411241.1:p.Cys64Tyr
ENST00000474030.5:n.274G>A
NM_000312.3:c.191G>A , LRG_599t1:c.191G>A NP_000303.1:p.Cys64Tyr
XM_005263715.3:c.374G>A XP_005263772.1:p.Cys125Tyr
XM_005263716.3:c.254G>A XP_005263773.1:p.Cys85Tyr
XM_005263717.3:c.254G>A XP_005263774.1:p.Cys85Tyr
XM_005263717.4:c.254G>A XP_005263774.1:p.Cys85Tyr
XM_017004505.1:c.434G>A XP_016859994.1:p.Cys145Tyr
XM_024453002.1:c.434G>A XP_024308770.1:p.Cys145Tyr
XM_024453003.1:c.374G>A XP_024308771.1:p.Cys125Tyr
XM_024453004.1:c.374G>A XP_024308772.1:p.Cys125Tyr
XM_024453005.1:c.254G>A XP_024308773.1:p.Cys85Tyr
XM_024453006.1:c.191G>A XP_024308774.1:p.Cys64Tyr
NM_000312.4:c.191G>A MANE Select NP_000303.1:p.Cys64Tyr
NM_001375602.1:c.374G>A NP_001362531.1:p.Cys125Tyr
NM_001375603.1:c.254G>A NP_001362532.1:p.Cys85Tyr
NM_001375604.1:c.254G>A NP_001362533.1:p.Cys85Tyr
NM_001375605.1:c.191G>A NP_001362534.1:p.Cys64Tyr
NM_001375606.1:c.254G>A NP_001362535.1:p.Cys85Tyr
NM_001375607.1:c.275G>A NP_001362536.1:p.Cys92Tyr
NM_001375608.1:c.191G>A NP_001362537.1:p.Cys64Tyr
NM_001375609.1:c.167G>A NP_001362538.1:p.Cys56Tyr
NM_001375610.1:c.185G>A NP_001362539.1:p.Cys62Tyr
NM_001375611.1:c.191G>A NP_001362540.1:p.Cys64Tyr
NM_001375613.1:c.191G>A NP_001362542.1:p.Cys64Tyr