Canonical Allele Identifier: CA2575831471

Gene: ANPEP

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89792124_89792125del , CM000677.2:g.89792124_89792125del	GRCh38
NC_000015.9:g.90335355_90335356del , CM000677.1:g.90335355_90335356del	GRCh37
NC_000015.8:g.88136359_88136360del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300060.7:c.2528+38_2528+39del MANE Select	ENSP00000300060.6:n.2528+38_2528+39del
ENST00000559874.2:c.2528+38_2528+39del	ENSP00000452934.2:n.2528+38_2528+39del
ENST00000560137.2:c.2528+38_2528+39del	ENSP00000453413.2:n.2528+38_2528+39del
ENST00000679248.1:c.2528+38_2528+39del	ENSP00000502886.1:n.2528+38_2528+39del
ENST00000300060.6:c.2528+38_2528+39del	ENSP00000300060.6:n.2528+38_2528+39del
ENST00000558740.1:n.432+38_432+39del
NM_001150.2:c.2528+38_2528+39del	NP_001141.2:n.2528+38_2528+39del
XM_005254892.3:c.2528+38_2528+39del	XP_005254949.1:n.2528+38_2528+39del
XM_011521473.1:c.2528+38_2528+39del	XP_011519775.1:n.2528+38_2528+39del
XM_005254892.4:c.2528+38_2528+39del	XP_005254949.1:n.2528+38_2528+39del
NM_001150.3:c.2528+38_2528+39del MANE Select	NP_001141.2:n.2528+38_2528+39del
NM_001381923.1:c.2528+38_2528+39del	NP_001368852.1:n.2528+38_2528+39del
NM_001381924.1:c.2528+38_2528+39del	NP_001368853.1:n.2528+38_2528+39del