Canonical Allele Identifier: CA2577090359
Gene: PROC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127426164_127426166del , CM000664.2:g.127426164_127426166del GRCh38
NC_000002.11:g.128183740_128183742del , CM000664.1:g.128183740_128183742del GRCh37
NC_000002.10:g.127900210_127900212del NCBI36
NG_016323.1:g.12745_12747del , LRG_599:g.12745_12747del

Transcript Alleles

HGVS Amino-acid Change
ENST00000234071.8:c.615_617del MANE Select ENSP00000234071.4:p.Glu205del
ENST00000234071.7:c.615_617del ENSP00000234071.3:p.Glu205del
ENST00000402125.2:c.121-2193_121-2191del
ENST00000409048.1:c.717_719del ENSP00000386679.1:p.Glu239del
ENST00000464089.1:n.201_203del
NM_000312.3:c.615_617del , LRG_599t1:c.615_617del NP_000303.1:p.Glu205del
XM_005263715.3:c.798_800del XP_005263772.1:p.Glu266del
XM_005263716.3:c.780_782del XP_005263773.1:p.Glu260del
XM_005263717.3:c.678_680del XP_005263774.1:p.Glu226del
XM_005263717.4:c.678_680del XP_005263774.1:p.Glu226del
XM_017004505.1:c.858_860del XP_016859994.1:p.Glu286del
XM_024453002.1:c.960_962del XP_024308770.1:p.Glu320del
XM_024453003.1:c.900_902del XP_024308771.1:p.Glu300del
XM_024453004.1:c.798_800del XP_024308772.1:p.Glu266del
XM_024453005.1:c.780_782del XP_024308773.1:p.Glu260del
XM_024453006.1:c.717_719del XP_024308774.1:p.Glu239del
XR_923313.2:n.4423_4425del
NM_000312.4:c.615_617del MANE Select NP_000303.1:p.Glu205del
NM_001375602.1:c.798_800del NP_001362531.1:p.Glu266del
NM_001375603.1:c.780_782del NP_001362532.1:p.Glu260del
NM_001375604.1:c.678_680del NP_001362533.1:p.Glu226del
NM_001375605.1:c.717_719del NP_001362534.1:p.Glu239del
NM_001375606.1:c.783_785del NP_001362535.1:p.Glu261del
NM_001375607.1:c.801_803del NP_001362536.1:p.Glu267del
NM_001375608.1:c.558_560del NP_001362537.1:p.Glu186del
NM_001375609.1:c.591_593del NP_001362538.1:p.Glu197del
NM_001375610.1:c.609_611del NP_001362539.1:p.Glu203del
NM_001375611.1:c.615_617del NP_001362540.1:p.Glu205del
NM_001375613.1:c.615_617del NP_001362542.1:p.Glu205del