Canonical Allele Identifier: CA2194795304
Gene: ANPEP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89792575T= , CM000677.2:g.89792575T= GRCh38
NC_000015.9:g.90335806T= , CM000677.1:g.90335806T= GRCh37
NC_000015.8:g.88136810T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000300060.7:c.2250-13A= MANE Select ENSP00000300060.6:n.2250-13A=
ENST00000559874.2:c.2250-13A= ENSP00000452934.2:n.2250-13A=
ENST00000560137.2:c.2250-13A= ENSP00000453413.2:n.2250-13A=
ENST00000679248.1:c.2250-13A= ENSP00000502886.1:n.2250-13A=
ENST00000300060.6:c.2250-13A= ENSP00000300060.6:n.2250-13A=
ENST00000558740.1:n.154-13A=
NM_001150.2:c.2250-13A= NP_001141.2:n.2250-13A=
XM_005254892.3:c.2250-13A= XP_005254949.1:n.2250-13A=
XM_011521473.1:c.2250-13A= XP_011519775.1:n.2250-13A=
XM_005254892.4:c.2250-13A= XP_005254949.1:n.2250-13A=
NM_001150.3:c.2250-13A= MANE Select NP_001141.2:n.2250-13A=
NM_001381923.1:c.2250-13A= NP_001368852.1:n.2250-13A=
NM_001381924.1:c.2250-13A= NP_001368853.1:n.2250-13A=