Canonical Allele Identifier: CA2586969897
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426116del , CM000664.2:g.127426116del GRCh38
NC_000002.11:g.128183692del , CM000664.1:g.128183692del GRCh37
NC_000002.10:g.127900162del NCBI36
NG_016323.1:g.12697del , LRG_599:g.12697del

Transcript Alleles

HGVS Amino-acid change
ENST00000234071.8:c.567del MANE Select ENSP00000234071.4:p.Met190TrpfsTer8
ENST00000234071.7:c.567del ENSP00000234071.3:p.Met190TrpfsTer8
ENST00000402125.2:c.121-2241del
ENST00000409048.1:c.669del ENSP00000386679.1:p.Met224TrpfsTer8
ENST00000442644.5:c.510del ENSP00000411241.1:p.Met171TrpfsTer?
ENST00000464089.1:n.153del
NM_000312.3:c.567del , LRG_599t1:c.567del NP_000303.1:p.Met190TrpfsTer8
XM_005263715.3:c.750del XP_005263772.1:p.Met251TrpfsTer8
XM_005263716.3:c.732del XP_005263773.1:p.Met245TrpfsTer8
XM_005263717.3:c.630del XP_005263774.1:p.Met211TrpfsTer8
XM_005263717.4:c.630del XP_005263774.1:p.Met211TrpfsTer8
XM_017004505.1:c.810del XP_016859994.1:p.Met271TrpfsTer8
XM_024453002.1:c.912del XP_024308770.1:p.Met305TrpfsTer8
XM_024453003.1:c.852del XP_024308771.1:p.Met285TrpfsTer8
XM_024453004.1:c.750del XP_024308772.1:p.Met251TrpfsTer8
XM_024453005.1:c.732del XP_024308773.1:p.Met245TrpfsTer8
XM_024453006.1:c.669del XP_024308774.1:p.Met224TrpfsTer8
XR_923313.2:n.4470del
NM_000312.4:c.567del MANE Select NP_000303.1:p.Met190TrpfsTer8
NM_001375602.1:c.750del NP_001362531.1:p.Met251TrpfsTer8
NM_001375603.1:c.732del NP_001362532.1:p.Met245TrpfsTer8
NM_001375604.1:c.630del NP_001362533.1:p.Met211TrpfsTer8
NM_001375605.1:c.669del NP_001362534.1:p.Met224TrpfsTer8
NM_001375606.1:c.735del NP_001362535.1:p.Met246TrpfsTer8
NM_001375607.1:c.753del NP_001362536.1:p.Met252TrpfsTer8
NM_001375608.1:c.510del NP_001362537.1:p.Met171TrpfsTer8
NM_001375609.1:c.543del NP_001362538.1:p.Met182TrpfsTer8
NM_001375610.1:c.561del NP_001362539.1:p.Met188TrpfsTer8
NM_001375611.1:c.567del NP_001362540.1:p.Met190TrpfsTer8
NM_001375613.1:c.567del NP_001362542.1:p.Met190TrpfsTer8