Canonical Allele Identifier: CA155829717

Gene: NPY

Linked Data

• dbSNP Id: rs562670318
• gnomAD v2: 7-24330445-GCA-G
• gnomAD v3: 7-24290826-GCA-G
• gnomAD v4: 7-24290826-GCA-G
• MyVariant Identifiers: chr7:g.24330446_24330447del (hg19) ; chr7:g.24290827_24290828del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290829_24290830del , CM000669.2:g.24290829_24290830del	GRCh38
NC_000007.13:g.24330448_24330449del , CM000669.1:g.24330448_24330449del	GRCh37
NC_000007.12:g.24296973_24296974del	NCBI36
NG_016148.1:g.11642_11643del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-834_270-833del MANE Select	ENSP00000242152.2:n.270-834_270-833del
ENST00000242152.6:c.270-834_270-833del	ENSP00000242152.2:n.270-834_270-833del
ENST00000405982.1:c.270-834_270-833del	ENSP00000385282.1:n.270-834_270-833del
ENST00000407573.5:c.270-834_270-833del	ENSP00000384364.1:n.270-834_270-833del
NM_000905.3:c.270-834_270-833del	NP_000896.1:n.270-834_270-833del
XM_017012910.1:c.41+28529_41+28530del	XP_016868399.1:n.41+28529_41+28530del
XM_017012911.1:c.41+28529_41+28530del	XP_016868400.1:n.41+28529_41+28530del
XR_001745121.1:n.473+28529_473+28530del
XR_001745122.1:n.345-93799_345-93798del
XR_001745123.1:n.473+28529_473+28530del
XR_001745124.1:n.473+28529_473+28530del
XR_001745125.1:n.473+28529_473+28530del
XR_001745126.1:n.473+28529_473+28530del
XR_001745127.1:n.345-35129_345-35128del
XR_001745129.1:n.473+28529_473+28530del
XR_001745130.1:n.473+28529_473+28530del
XR_001745131.1:n.473+28529_473+28530del
XR_001745132.1:n.473+28529_473+28530del
NM_000905.4:c.270-834_270-833del MANE Select	NP_000896.1:n.270-834_270-833del