Canonical Allele Identifier: CA1099401097

Gene: NPY

Linked Data

• gnomAD v3: 7-24290778-T-TA
• gnomAD v4: 7-24290778-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290779dup , CM000669.2:g.24290779dup	GRCh38
NC_000007.13:g.24330398dup , CM000669.1:g.24330398dup	GRCh37
NC_000007.12:g.24296923dup	NCBI36
NG_016148.1:g.11592dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-884dup MANE Select	ENSP00000242152.2:n.270-884dup
ENST00000242152.6:c.270-884dup	ENSP00000242152.2:n.270-884dup
ENST00000405982.1:c.270-884dup	ENSP00000385282.1:n.270-884dup
ENST00000407573.5:c.270-884dup	ENSP00000384364.1:n.270-884dup
NM_000905.3:c.270-884dup	NP_000896.1:n.270-884dup
XM_017012910.1:c.41+28578dup	XP_016868399.1:n.41+28578dup
XM_017012911.1:c.41+28578dup	XP_016868400.1:n.41+28578dup
XR_001745121.1:n.473+28578dup
XR_001745122.1:n.345-93750dup
XR_001745123.1:n.473+28578dup
XR_001745124.1:n.473+28578dup
XR_001745125.1:n.473+28578dup
XR_001745126.1:n.473+28578dup
XR_001745127.1:n.345-35080dup
XR_001745129.1:n.473+28578dup
XR_001745130.1:n.473+28578dup
XR_001745131.1:n.473+28578dup
XR_001745132.1:n.473+28578dup
NM_000905.4:c.270-884dup MANE Select	NP_000896.1:n.270-884dup