Canonical Allele Identifier: CA7730864
Gene: ANPEP HGNC NCBI

Linked Data

ClinVar Variation Id: 2459909
ClinVar RCV Id: RCV004249285
dbSNP Id: rs1803098

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89792555C>T , CM000677.2:g.89792555C>T GRCh38
NC_000015.9:g.90335786C>T , CM000677.1:g.90335786C>T GRCh37
NC_000015.8:g.88136790C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000300060.7:c.2257G>A MANE Select ENSP00000300060.6:p.Glu753Lys
ENST00000559874.2:c.2257G>A ENSP00000452934.2:p.Glu753Lys
ENST00000560137.2:c.2257G>A ENSP00000453413.2:p.Glu753Lys
ENST00000679248.1:c.2257G>A ENSP00000502886.1:p.Glu753Lys
ENST00000300060.6:c.2257G>A ENSP00000300060.6:p.Glu753Lys
ENST00000558740.1:n.161G>A
NM_001150.2:c.2257G>A NP_001141.2:p.Glu753Lys
XM_005254892.3:c.2257G>A XP_005254949.1:p.Glu753Lys
XM_011521473.1:c.2257G>A XP_011519775.1:p.Glu753Lys
XM_005254892.4:c.2257G>A XP_005254949.1:p.Glu753Lys
NM_001150.3:c.2257G>A MANE Select NP_001141.2:p.Glu753Lys
NM_001381923.1:c.2257G>A NP_001368852.1:p.Glu753Lys
NM_001381924.1:c.2257G>A NP_001368853.1:p.Glu753Lys