Canonical Allele Identifier: CA716977768

Gene: ANPEP

Linked Data

• dbSNP Id: rs1322013389
• gnomAD v4: 15-89792371-G-A
• MyVariant Identifiers: chr15:g.90335602G>A (hg19) ; chr15:g.89792371G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89792371G>A , CM000677.2:g.89792371G>A	GRCh38
NC_000015.9:g.90335602G>A , CM000677.1:g.90335602G>A	GRCh37
NC_000015.8:g.88136606G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300060.7:c.2361-44C>T MANE Select	ENSP00000300060.6:n.2361-44C>T
ENST00000559874.2:c.2361-44C>T	ENSP00000452934.2:n.2361-44C>T
ENST00000560137.2:c.2361-44C>T	ENSP00000453413.2:n.2361-44C>T
ENST00000679248.1:c.2361-44C>T	ENSP00000502886.1:n.2361-44C>T
ENST00000300060.6:c.2361-44C>T	ENSP00000300060.6:n.2361-44C>T
ENST00000558740.1:n.265-44C>T
NM_001150.2:c.2361-44C>T	NP_001141.2:n.2361-44C>T
XM_005254892.3:c.2361-44C>T	XP_005254949.1:n.2361-44C>T
XM_011521473.1:c.2361-44C>T	XP_011519775.1:n.2361-44C>T
XM_005254892.4:c.2361-44C>T	XP_005254949.1:n.2361-44C>T
NM_001150.3:c.2361-44C>T MANE Select	NP_001141.2:n.2361-44C>T
NM_001381923.1:c.2361-44C>T	NP_001368852.1:n.2361-44C>T
NM_001381924.1:c.2361-44C>T	NP_001368853.1:n.2361-44C>T