Canonical Allele Identifier: CA2194794722

Gene: ANPEP

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89792249_89792258delinsCCAGGCGAAG , CM000677.2:g.89792249_89792258delinsCCAGGCGAAG	GRCh38
NC_000015.9:g.90335480_90335489delinsCCAGGCGAAG , CM000677.1:g.90335480_90335489delinsCCAGGCGAAG	GRCh37
NC_000015.8:g.88136484_88136493delinsCCAGGCGAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300060.7:c.2430_2439delinsCTTCGCCTGG MANE Select	ENSP00000300060.6:p.Asp810=
ENST00000559874.2:c.2430_2439delinsCTTCGCCTGG	ENSP00000452934.2:p.Asp810=
ENST00000560137.2:c.2430_2439delinsCTTCGCCTGG	ENSP00000453413.2:p.Asp810=
ENST00000679248.1:c.2430_2439delinsCTTCGCCTGG	ENSP00000502886.1:p.Asp810=
ENST00000300060.6:c.2430_2439delinsCTTCGCCTGG	ENSP00000300060.6:p.Asp810=
ENST00000558740.1:n.334_343delinsCTTCGCCTGG
NM_001150.2:c.2430_2439delinsCTTCGCCTGG	NP_001141.2:p.Asp810=
XM_005254892.3:c.2430_2439delinsCTTCGCCTGG	XP_005254949.1:p.Asp810=
XM_011521473.1:c.2430_2439delinsCTTCGCCTGG	XP_011519775.1:p.Asp810=
XM_005254892.4:c.2430_2439delinsCTTCGCCTGG	XP_005254949.1:p.Asp810=
NM_001150.3:c.2430_2439delinsCTTCGCCTGG MANE Select	NP_001141.2:p.Asp810=
NM_001381923.1:c.2430_2439delinsCTTCGCCTGG	NP_001368852.1:p.Asp810=
NM_001381924.1:c.2430_2439delinsCTTCGCCTGG	NP_001368853.1:p.Asp810=