Canonical Allele Identifier: CA2194794776
Gene: ANPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89792271_89792272delinsTC , CM000677.2:g.89792271_89792272delinsTC GRCh38
NC_000015.9:g.90335502_90335503delinsTC , CM000677.1:g.90335502_90335503delinsTC GRCh37
NC_000015.8:g.88136506_88136507delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000300060.7:c.2416_2417delinsGA MANE Select ENSP00000300060.6:p.Glu806=
ENST00000559874.2:c.2416_2417delinsGA ENSP00000452934.2:p.Glu806=
ENST00000560137.2:c.2416_2417delinsGA ENSP00000453413.2:p.Glu806=
ENST00000679248.1:c.2416_2417delinsGA ENSP00000502886.1:p.Glu806=
ENST00000300060.6:c.2416_2417delinsGA ENSP00000300060.6:p.Glu806=
ENST00000558740.1:n.320_321delinsGA
NM_001150.2:c.2416_2417delinsGA NP_001141.2:p.Glu806=
XM_005254892.3:c.2416_2417delinsGA XP_005254949.1:p.Glu806=
XM_011521473.1:c.2416_2417delinsGA XP_011519775.1:p.Glu806=
XM_005254892.4:c.2416_2417delinsGA XP_005254949.1:p.Glu806=
NM_001150.3:c.2416_2417delinsGA MANE Select NP_001141.2:p.Glu806=
NM_001381923.1:c.2416_2417delinsGA NP_001368852.1:p.Glu806=
NM_001381924.1:c.2416_2417delinsGA NP_001368853.1:p.Glu806=