Canonical Allele Identifier: CA2630295440
Gene: ANPEP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89792075del , CM000677.2:g.89792075del GRCh38
NC_000015.9:g.90335306del , CM000677.1:g.90335306del GRCh37
NC_000015.8:g.88136310del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000300060.7:c.2528+86del MANE Select ENSP00000300060.6:n.2528+86del
ENST00000559874.2:c.2528+86del ENSP00000452934.2:n.2528+86del
ENST00000560137.2:c.2528+86del ENSP00000453413.2:n.2528+86del
ENST00000679248.1:c.2528+86del ENSP00000502886.1:n.2528+86del
ENST00000300060.6:c.2528+86del ENSP00000300060.6:n.2528+86del
ENST00000558740.1:n.432+86del
NM_001150.2:c.2528+86del NP_001141.2:n.2528+86del
XM_005254892.3:c.2528+86del XP_005254949.1:n.2528+86del
XM_011521473.1:c.2528+86del XP_011519775.1:n.2528+86del
XM_005254892.4:c.2528+86del XP_005254949.1:n.2528+86del
NM_001150.3:c.2528+86del MANE Select NP_001141.2:n.2528+86del
NM_001381923.1:c.2528+86del NP_001368852.1:n.2528+86del
NM_001381924.1:c.2528+86del NP_001368853.1:n.2528+86del