Canonical Allele Identifier: CA573375197

Gene: NPY

Linked Data

• dbSNP Id: rs1205410654
• gnomAD v2: 7-24330389-A-AT
• gnomAD v3: 7-24290770-A-AT
• gnomAD v4: 7-24290770-A-AT
• MyVariant Identifiers: chr7:g.24330389_24330390insT (hg19) ; chr7:g.24290770_24290771insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290771dup , CM000669.2:g.24290771dup	GRCh38
NC_000007.13:g.24330390dup , CM000669.1:g.24330390dup	GRCh37
NC_000007.12:g.24296915dup	NCBI36
NG_016148.1:g.11584dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-892dup MANE Select	ENSP00000242152.2:n.270-892dup
ENST00000242152.6:c.270-892dup	ENSP00000242152.2:n.270-892dup
ENST00000405982.1:c.270-892dup	ENSP00000385282.1:n.270-892dup
ENST00000407573.5:c.270-892dup	ENSP00000384364.1:n.270-892dup
NM_000905.3:c.270-892dup	NP_000896.1:n.270-892dup
XM_017012910.1:c.41+28586dup	XP_016868399.1:n.41+28586dup
XM_017012911.1:c.41+28586dup	XP_016868400.1:n.41+28586dup
XR_001745121.1:n.473+28586dup
XR_001745122.1:n.345-93742dup
XR_001745123.1:n.473+28586dup
XR_001745124.1:n.473+28586dup
XR_001745125.1:n.473+28586dup
XR_001745126.1:n.473+28586dup
XR_001745127.1:n.345-35072dup
XR_001745129.1:n.473+28586dup
XR_001745130.1:n.473+28586dup
XR_001745131.1:n.473+28586dup
XR_001745132.1:n.473+28586dup
NM_000905.4:c.270-892dup MANE Select	NP_000896.1:n.270-892dup