Canonical Allele Identifier: CA619859084

Gene: ANPEP

Linked Data

• dbSNP Id: rs1313756707
• gnomAD v2: 15-90335564-G-GT
• gnomAD v4: 15-89792333-G-GT
• MyVariant Identifiers: chr15:g.90335564_90335565insT (hg19) ; chr15:g.89792333_89792334insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89792334dup , CM000677.2:g.89792334dup	GRCh38
NC_000015.9:g.90335565dup , CM000677.1:g.90335565dup	GRCh37
NC_000015.8:g.88136569dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300060.7:c.2361-7dup MANE Select	ENSP00000300060.6:n.2361-7dup
ENST00000559874.2:c.2361-7dup	ENSP00000452934.2:n.2361-7dup
ENST00000560137.2:c.2361-7dup	ENSP00000453413.2:n.2361-7dup
ENST00000679248.1:c.2361-7dup	ENSP00000502886.1:n.2361-7dup
ENST00000300060.6:c.2361-7dup	ENSP00000300060.6:n.2361-7dup
ENST00000558740.1:n.265-7dup
NM_001150.2:c.2361-7dup	NP_001141.2:n.2361-7dup
XM_005254892.3:c.2361-7dup	XP_005254949.1:n.2361-7dup
XM_011521473.1:c.2361-7dup	XP_011519775.1:n.2361-7dup
XM_005254892.4:c.2361-7dup	XP_005254949.1:n.2361-7dup
NM_001150.3:c.2361-7dup MANE Select	NP_001141.2:n.2361-7dup
NM_001381923.1:c.2361-7dup	NP_001368852.1:n.2361-7dup
NM_001381924.1:c.2361-7dup	NP_001368853.1:n.2361-7dup