Canonical Allele Identifier: CA2630296436

Gene: ANPEP

Linked Data

• gnomAD v4: 15-89792939-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89792939_89792940insA , CM000677.2:g.89792939_89792940insA	GRCh38
NC_000015.9:g.90336170_90336171insA , CM000677.1:g.90336170_90336171insA	GRCh37
NC_000015.8:g.88137174_88137175insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300060.7:c.2249+95_2249+96insT MANE Select	ENSP00000300060.6:n.2249+95_2249+96insT
ENST00000559874.2:c.2249+95_2249+96insT	ENSP00000452934.2:n.2249+95_2249+96insT
ENST00000560137.2:c.2249+95_2249+96insT	ENSP00000453413.2:n.2249+95_2249+96insT
ENST00000679248.1:c.2249+95_2249+96insT	ENSP00000502886.1:n.2249+95_2249+96insT
ENST00000300060.6:c.2249+95_2249+96insT	ENSP00000300060.6:n.2249+95_2249+96insT
ENST00000558740.1:n.153+95_153+96insT
NM_001150.2:c.2249+95_2249+96insT	NP_001141.2:n.2249+95_2249+96insT
XM_005254892.3:c.2249+95_2249+96insT	XP_005254949.1:n.2249+95_2249+96insT
XM_011521473.1:c.2249+95_2249+96insT	XP_011519775.1:n.2249+95_2249+96insT
XM_005254892.4:c.2249+95_2249+96insT	XP_005254949.1:n.2249+95_2249+96insT
NM_001150.3:c.2249+95_2249+96insT MANE Select	NP_001141.2:n.2249+95_2249+96insT
NM_001381923.1:c.2249+95_2249+96insT	NP_001368852.1:n.2249+95_2249+96insT
NM_001381924.1:c.2249+95_2249+96insT	NP_001368853.1:n.2249+95_2249+96insT