Canonical Allele Identifier: CA573375191

Gene: NPY

Linked Data

• dbSNP Id: rs747171869
• gnomAD v2: 7-24330378-A-AAATAATAATAAT
• gnomAD v3: 7-24290759-A-AAATAATAATAAT
• gnomAD v4: 7-24290759-A-AAATAATAATAAT
• MyVariant Identifiers: chr7:g.24330381_24330382insAATAATAATAAT (hg19) ; chr7:g.24330378_24330379insAATAATAATAAT (hg19) ; chr7:g.24290762_24290763insAATAATAATAAT (hg38) ; chr7:g.24290759_24290760insAATAATAATAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290766_24290777dup , CM000669.2:g.24290766_24290777dup	GRCh38
NC_000007.13:g.24330385_24330396dup , CM000669.1:g.24330385_24330396dup	GRCh37
NC_000007.12:g.24296910_24296921dup	NCBI36
NG_016148.1:g.11579_11590dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-897_270-886dup MANE Select	ENSP00000242152.2:n.270-897_270-886dup
ENST00000242152.6:c.270-897_270-886dup	ENSP00000242152.2:n.270-897_270-886dup
ENST00000405982.1:c.270-897_270-886dup	ENSP00000385282.1:n.270-897_270-886dup
ENST00000407573.5:c.270-897_270-886dup	ENSP00000384364.1:n.270-897_270-886dup
NM_000905.3:c.270-897_270-886dup	NP_000896.1:n.270-897_270-886dup
XM_017012910.1:c.41+28586_41+28597dup	XP_016868399.1:n.41+28586_41+28597dup
XM_017012911.1:c.41+28586_41+28597dup	XP_016868400.1:n.41+28586_41+28597dup
XR_001745121.1:n.473+28586_473+28597dup
XR_001745122.1:n.345-93742_345-93731dup
XR_001745123.1:n.473+28586_473+28597dup
XR_001745124.1:n.473+28586_473+28597dup
XR_001745125.1:n.473+28586_473+28597dup
XR_001745126.1:n.473+28586_473+28597dup
XR_001745127.1:n.345-35072_345-35061dup
XR_001745129.1:n.473+28586_473+28597dup
XR_001745130.1:n.473+28586_473+28597dup
XR_001745131.1:n.473+28586_473+28597dup
XR_001745132.1:n.473+28586_473+28597dup
NM_000905.4:c.270-897_270-886dup MANE Select	NP_000896.1:n.270-897_270-886dup