Canonical Allele Identifier: CA2630295614

Gene: ANPEP

Linked Data

• gnomAD v4: 15-89792201-C-CCGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89792203_89792204insCTCG , CM000677.2:g.89792203_89792204insCTCG	GRCh38
NC_000015.9:g.90335434_90335435insCTCG , CM000677.1:g.90335434_90335435insCTCG	GRCh37
NC_000015.8:g.88136438_88136439insCTCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300060.7:c.2486_2487insAGCG MANE Select	ENSP00000300060.6:p.Ala831GlyfsTer?
ENST00000559874.2:c.2486_2487insAGCG	ENSP00000452934.2:p.Ala831GlyfsTer?
ENST00000560137.2:c.2486_2487insAGCG	ENSP00000453413.2:p.Ala831GlyfsTer?
ENST00000679248.1:c.2486_2487insAGCG	ENSP00000502886.1:p.Ala831GlyfsTer?
ENST00000300060.6:c.2486_2487insAGCG	ENSP00000300060.6:p.Ala831GlyfsTer?
ENST00000558740.1:n.390_391insAGCG
NM_001150.2:c.2486_2487insAGCG	NP_001141.2:p.Ala831GlyfsTer?
XM_005254892.3:c.2486_2487insAGCG	XP_005254949.1:p.Ala831GlyfsTer?
XM_011521473.1:c.2486_2487insAGCG	XP_011519775.1:p.Ala831GlyfsTer?
XM_005254892.4:c.2486_2487insAGCG	XP_005254949.1:p.Ala831GlyfsTer?
NM_001150.3:c.2486_2487insAGCG MANE Select	NP_001141.2:p.Ala831GlyfsTer?
NM_001381923.1:c.2486_2487insAGCG	NP_001368852.1:p.Ala831GlyfsTer?
NM_001381924.1:c.2486_2487insAGCG	NP_001368853.1:p.Ala831GlyfsTer?