Canonical Allele Identifier: CA2194795425
Gene: ANPEP HGNC NCBI

Linked Data

dbSNP Id: rs1968654751

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89792650_89792651insTGG , CM000677.2:g.89792650_89792651insTGG GRCh38
NC_000015.9:g.90335881_90335882insTGG , CM000677.1:g.90335881_90335882insTGG GRCh37
NC_000015.8:g.88136885_88136886insTGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000300060.7:c.2250-88_2250-87insCAC MANE Select ENSP00000300060.6:n.2250-88_2250-87insCAC
ENST00000559874.2:c.2250-88_2250-87insCAC ENSP00000452934.2:n.2250-88_2250-87insCAC
ENST00000560137.2:c.2250-88_2250-87insCAC ENSP00000453413.2:n.2250-88_2250-87insCAC
ENST00000679248.1:c.2250-88_2250-87insCAC ENSP00000502886.1:n.2250-88_2250-87insCAC
ENST00000300060.6:c.2250-88_2250-87insCAC ENSP00000300060.6:n.2250-88_2250-87insCAC
ENST00000558740.1:n.154-88_154-87insCAC
NM_001150.2:c.2250-88_2250-87insCAC NP_001141.2:n.2250-88_2250-87insCAC
XM_005254892.3:c.2250-88_2250-87insCAC XP_005254949.1:n.2250-88_2250-87insCAC
XM_011521473.1:c.2250-88_2250-87insCAC XP_011519775.1:n.2250-88_2250-87insCAC
XM_005254892.4:c.2250-88_2250-87insCAC XP_005254949.1:n.2250-88_2250-87insCAC
NM_001150.3:c.2250-88_2250-87insCAC MANE Select NP_001141.2:n.2250-88_2250-87insCAC
NM_001381923.1:c.2250-88_2250-87insCAC NP_001368852.1:n.2250-88_2250-87insCAC
NM_001381924.1:c.2250-88_2250-87insCAC NP_001368853.1:n.2250-88_2250-87insCAC