Canonical Allele Identifier: CA1099401094

Gene: NPY

Linked Data

• dbSNP Id: rs1787574180
• gnomAD v3: 7-24290777-T-TAA
• gnomAD v4: 7-24290777-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290777_24290778insAA , CM000669.2:g.24290777_24290778insAA	GRCh38
NC_000007.13:g.24330396_24330397insAA , CM000669.1:g.24330396_24330397insAA	GRCh37
NC_000007.12:g.24296921_24296922insAA	NCBI36
NG_016148.1:g.11590_11591insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-886_270-885insAA MANE Select	ENSP00000242152.2:n.270-886_270-885insAA
ENST00000242152.6:c.270-886_270-885insAA	ENSP00000242152.2:n.270-886_270-885insAA
ENST00000405982.1:c.270-886_270-885insAA	ENSP00000385282.1:n.270-886_270-885insAA
ENST00000407573.5:c.270-886_270-885insAA	ENSP00000384364.1:n.270-886_270-885insAA
NM_000905.3:c.270-886_270-885insAA	NP_000896.1:n.270-886_270-885insAA
XM_017012910.1:c.41+28579_41+28580insTT	XP_016868399.1:n.41+28579_41+28580insTT
XM_017012911.1:c.41+28579_41+28580insTT	XP_016868400.1:n.41+28579_41+28580insTT
XR_001745121.1:n.473+28579_473+28580insTT
XR_001745122.1:n.345-93749_345-93748insTT
XR_001745123.1:n.473+28579_473+28580insTT
XR_001745124.1:n.473+28579_473+28580insTT
XR_001745125.1:n.473+28579_473+28580insTT
XR_001745126.1:n.473+28579_473+28580insTT
XR_001745127.1:n.345-35079_345-35078insTT
XR_001745129.1:n.473+28579_473+28580insTT
XR_001745130.1:n.473+28579_473+28580insTT
XR_001745131.1:n.473+28579_473+28580insTT
XR_001745132.1:n.473+28579_473+28580insTT
NM_000905.4:c.270-886_270-885insAA MANE Select	NP_000896.1:n.270-886_270-885insAA