Canonical Allele Identifier: CA1286884601
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428715G= , CM000664.2:g.127428715G= GRCh38
NC_000002.11:g.128186291G= , CM000664.1:g.128186291G= GRCh37
NC_000002.10:g.127902761G= NCBI36
NG_016323.1:g.15296G= , LRG_599:g.15296G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.1155G= MANE Select ENSP00000234071.4:p.Met385=
ENST00000234071.7:c.1155G= ENSP00000234071.3:p.Met385=
ENST00000402125.2:c.479G=
ENST00000409048.1:c.1257G= ENSP00000386679.1:p.Met419=
NM_000312.3:c.1155G= , LRG_599t1:c.1155G= NP_000303.1:p.Met385=
XM_005263715.3:c.1338G= XP_005263772.1:p.Met446=
XM_005263716.3:c.1320G= XP_005263773.1:p.Met440=
XM_005263717.3:c.1218G= XP_005263774.1:p.Met406=
XR_923313.1:n.1332-451C=
XM_005263717.4:c.1218G= XP_005263774.1:p.Met406=
XM_017004505.1:c.1398G= XP_016859994.1:p.Met466=
XM_024453002.1:c.1500G= XP_024308770.1:p.Met500=
XM_024453003.1:c.1440G= XP_024308771.1:p.Met480=
XM_024453004.1:c.1338G= XP_024308772.1:p.Met446=
XM_024453005.1:c.1320G= XP_024308773.1:p.Met440=
XM_024453006.1:c.1257G= XP_024308774.1:p.Met419=
XR_001739705.1:n.3607-451C=
XR_923313.2:n.4043-451C=
NM_000312.4:c.1155G= MANE Select NP_000303.1:p.Met385=
NM_001375602.1:c.1338G= NP_001362531.1:p.Met446=
NM_001375603.1:c.1320G= NP_001362532.1:p.Met440=
NM_001375604.1:c.1218G= NP_001362533.1:p.Met406=
NM_001375605.1:c.1257G= NP_001362534.1:p.Met419=
NM_001375606.1:c.1323G= NP_001362535.1:p.Met441=
NM_001375607.1:c.1341G= NP_001362536.1:p.Met447=
NM_001375608.1:c.1098G= NP_001362537.1:p.Met366=
NM_001375609.1:c.1131G= NP_001362538.1:p.Met377=
NM_001375610.1:c.1149G= NP_001362539.1:p.Met383=
NM_001375611.1:c.1155G= NP_001362540.1:p.Met385=
NM_001375613.1:c.1155G= NP_001362542.1:p.Met385=