Canonical Allele Identifier: CA1286884555
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127428619G= , CM000664.2:g.127428619G= GRCh38
NC_000002.11:g.128186195G= , CM000664.1:g.128186195G= GRCh37
NC_000002.10:g.127902665G= NCBI36
NG_016323.1:g.15200G= , LRG_599:g.15200G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.1059G= MANE Select ENSP00000234071.4:p.Lys353=
ENST00000234071.7:c.1059G= ENSP00000234071.3:p.Lys353=
ENST00000402125.2:c.383G=
ENST00000409048.1:c.1161G= ENSP00000386679.1:p.Lys387=
NM_000312.3:c.1059G= , LRG_599t1:c.1059G= NP_000303.1:p.Lys353=
XM_005263715.3:c.1242G= XP_005263772.1:p.Lys414=
XM_005263716.3:c.1224G= XP_005263773.1:p.Lys408=
XM_005263717.3:c.1122G= XP_005263774.1:p.Lys374=
XR_923313.1:n.1332-355C=
XM_005263717.4:c.1122G= XP_005263774.1:p.Lys374=
XM_017004505.1:c.1302G= XP_016859994.1:p.Lys434=
XM_024453002.1:c.1404G= XP_024308770.1:p.Lys468=
XM_024453003.1:c.1344G= XP_024308771.1:p.Lys448=
XM_024453004.1:c.1242G= XP_024308772.1:p.Lys414=
XM_024453005.1:c.1224G= XP_024308773.1:p.Lys408=
XM_024453006.1:c.1161G= XP_024308774.1:p.Lys387=
XR_001739705.1:n.3607-355C=
XR_923313.2:n.4043-355C=
NM_000312.4:c.1059G= MANE Select NP_000303.1:p.Lys353=
NM_001375602.1:c.1242G= NP_001362531.1:p.Lys414=
NM_001375603.1:c.1224G= NP_001362532.1:p.Lys408=
NM_001375604.1:c.1122G= NP_001362533.1:p.Lys374=
NM_001375605.1:c.1161G= NP_001362534.1:p.Lys387=
NM_001375606.1:c.1227G= NP_001362535.1:p.Lys409=
NM_001375607.1:c.1245G= NP_001362536.1:p.Lys415=
NM_001375608.1:c.1002G= NP_001362537.1:p.Lys334=
NM_001375609.1:c.1035G= NP_001362538.1:p.Lys345=
NM_001375610.1:c.1053G= NP_001362539.1:p.Lys351=
NM_001375611.1:c.1059G= NP_001362540.1:p.Lys353=
NM_001375613.1:c.1059G= NP_001362542.1:p.Lys353=