Canonical Allele Identifier: CA7730843
Gene: ANPEP HGNC NCBI

Linked Data

dbSNP Id: rs780695037

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89792437_89792438dup , CM000677.2:g.89792437_89792438dup GRCh38
NC_000015.9:g.90335668_90335669dup , CM000677.1:g.90335668_90335669dup GRCh37
NC_000015.8:g.88136672_88136673dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000300060.7:c.2360+14_2360+15dup MANE Select ENSP00000300060.6:n.2360+14_2360+15dup
ENST00000559874.2:c.2360+14_2360+15dup ENSP00000452934.2:n.2360+14_2360+15dup
ENST00000560137.2:c.2360+14_2360+15dup ENSP00000453413.2:n.2360+14_2360+15dup
ENST00000679248.1:c.2360+14_2360+15dup ENSP00000502886.1:n.2360+14_2360+15dup
ENST00000300060.6:c.2360+14_2360+15dup ENSP00000300060.6:n.2360+14_2360+15dup
ENST00000558740.1:n.264+14_264+15dup
NM_001150.2:c.2360+14_2360+15dup NP_001141.2:n.2360+14_2360+15dup
XM_005254892.3:c.2360+14_2360+15dup XP_005254949.1:n.2360+14_2360+15dup
XM_011521473.1:c.2360+14_2360+15dup XP_011519775.1:n.2360+14_2360+15dup
XM_005254892.4:c.2360+14_2360+15dup XP_005254949.1:n.2360+14_2360+15dup
NM_001150.3:c.2360+14_2360+15dup MANE Select NP_001141.2:n.2360+14_2360+15dup
NM_001381923.1:c.2360+14_2360+15dup NP_001368852.1:n.2360+14_2360+15dup
NM_001381924.1:c.2360+14_2360+15dup NP_001368853.1:n.2360+14_2360+15dup