Canonical Allele Identifier: CA2194795138
Gene: ANPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89792471C= , CM000677.2:g.89792471C= GRCh38
NC_000015.9:g.90335702C= , CM000677.1:g.90335702C= GRCh37
NC_000015.8:g.88136706C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000300060.7:c.2341G= MANE Select ENSP00000300060.6:p.Glu781=
ENST00000559874.2:c.2341G= ENSP00000452934.2:p.Glu781=
ENST00000560137.2:c.2341G= ENSP00000453413.2:p.Glu781=
ENST00000679248.1:c.2341G= ENSP00000502886.1:p.Glu781=
ENST00000300060.6:c.2341G= ENSP00000300060.6:p.Glu781=
ENST00000558740.1:n.245G=
NM_001150.2:c.2341G= NP_001141.2:p.Glu781=
XM_005254892.3:c.2341G= XP_005254949.1:p.Glu781=
XM_011521473.1:c.2341G= XP_011519775.1:p.Glu781=
XM_005254892.4:c.2341G= XP_005254949.1:p.Glu781=
NM_001150.3:c.2341G= MANE Select NP_001141.2:p.Glu781=
NM_001381923.1:c.2341G= NP_001368852.1:p.Glu781=
NM_001381924.1:c.2341G= NP_001368853.1:p.Glu781=