Canonical Allele Identifier: CA7730879
Gene: ANPEP HGNC NCBI

Linked Data

dbSNP Id: rs769096484

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89792607_89792610dup , CM000677.2:g.89792607_89792610dup GRCh38
NC_000015.9:g.90335838_90335841dup , CM000677.1:g.90335838_90335841dup GRCh37
NC_000015.8:g.88136842_88136845dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000300060.7:c.2250-45_2250-42dup MANE Select ENSP00000300060.6:n.2250-45_2250-42dup
ENST00000559874.2:c.2250-45_2250-42dup ENSP00000452934.2:n.2250-45_2250-42dup
ENST00000560137.2:c.2250-45_2250-42dup ENSP00000453413.2:n.2250-45_2250-42dup
ENST00000679248.1:c.2250-45_2250-42dup ENSP00000502886.1:n.2250-45_2250-42dup
ENST00000300060.6:c.2250-45_2250-42dup ENSP00000300060.6:n.2250-45_2250-42dup
ENST00000558740.1:n.154-45_154-42dup
NM_001150.2:c.2250-45_2250-42dup NP_001141.2:n.2250-45_2250-42dup
XM_005254892.3:c.2250-45_2250-42dup XP_005254949.1:n.2250-45_2250-42dup
XM_011521473.1:c.2250-45_2250-42dup XP_011519775.1:n.2250-45_2250-42dup
XM_005254892.4:c.2250-45_2250-42dup XP_005254949.1:n.2250-45_2250-42dup
NM_001150.3:c.2250-45_2250-42dup MANE Select NP_001141.2:n.2250-45_2250-42dup
NM_001381923.1:c.2250-45_2250-42dup NP_001368852.1:n.2250-45_2250-42dup
NM_001381924.1:c.2250-45_2250-42dup NP_001368853.1:n.2250-45_2250-42dup