Canonical Allele Identifier: CA2194795343

Gene: ANPEP

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89792591_89792592delinsCA , CM000677.2:g.89792591_89792592delinsCA	GRCh38
NC_000015.9:g.90335822_90335823delinsCA , CM000677.1:g.90335822_90335823delinsCA	GRCh37
NC_000015.8:g.88136826_88136827delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300060.7:c.2250-30_2250-29delinsTG MANE Select	ENSP00000300060.6:n.2250-30_2250-29delinsTG
ENST00000559874.2:c.2250-30_2250-29delinsTG	ENSP00000452934.2:n.2250-30_2250-29delinsTG
ENST00000560137.2:c.2250-30_2250-29delinsTG	ENSP00000453413.2:n.2250-30_2250-29delinsTG
ENST00000679248.1:c.2250-30_2250-29delinsTG	ENSP00000502886.1:n.2250-30_2250-29delinsTG
ENST00000300060.6:c.2250-30_2250-29delinsTG	ENSP00000300060.6:n.2250-30_2250-29delinsTG
ENST00000558740.1:n.154-30_154-29delinsTG
NM_001150.2:c.2250-30_2250-29delinsTG	NP_001141.2:n.2250-30_2250-29delinsTG
XM_005254892.3:c.2250-30_2250-29delinsTG	XP_005254949.1:n.2250-30_2250-29delinsTG
XM_011521473.1:c.2250-30_2250-29delinsTG	XP_011519775.1:n.2250-30_2250-29delinsTG
XM_005254892.4:c.2250-30_2250-29delinsTG	XP_005254949.1:n.2250-30_2250-29delinsTG
NM_001150.3:c.2250-30_2250-29delinsTG MANE Select	NP_001141.2:n.2250-30_2250-29delinsTG
NM_001381923.1:c.2250-30_2250-29delinsTG	NP_001368852.1:n.2250-30_2250-29delinsTG
NM_001381924.1:c.2250-30_2250-29delinsTG	NP_001368853.1:n.2250-30_2250-29delinsTG