Canonical Allele Identifier: CA155829655

Gene: NPY

Linked Data

• dbSNP Id: rs894749335
• gnomAD v2: 7-24330001-C-T
• gnomAD v3: 7-24290382-C-T
• gnomAD v4: 7-24290382-C-T
• MyVariant Identifiers: chr7:g.24330001C>T (hg19) ; chr7:g.24290382C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290382C>T , CM000669.2:g.24290382C>T	GRCh38
NC_000007.13:g.24330001C>T , CM000669.1:g.24330001C>T	GRCh37
NC_000007.12:g.24296526C>T	NCBI36
NG_016148.1:g.11195C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.269+803C>T MANE Select	ENSP00000242152.2:n.269+803C>T
ENST00000242152.6:c.269+803C>T	ENSP00000242152.2:n.269+803C>T
ENST00000405982.1:c.269+803C>T	ENSP00000385282.1:n.269+803C>T
ENST00000407573.5:c.269+803C>T	ENSP00000384364.1:n.269+803C>T
NM_000905.3:c.269+803C>T	NP_000896.1:n.269+803C>T
XM_017012910.1:c.41+28975G>A	XP_016868399.1:n.41+28975G>A
XM_017012911.1:c.41+28975G>A	XP_016868400.1:n.41+28975G>A
XR_001745121.1:n.473+28975G>A
XR_001745122.1:n.345-93353G>A
XR_001745123.1:n.473+28975G>A
XR_001745124.1:n.473+28975G>A
XR_001745125.1:n.473+28975G>A
XR_001745126.1:n.473+28975G>A
XR_001745127.1:n.345-34683G>A
XR_001745129.1:n.473+28975G>A
XR_001745130.1:n.473+28975G>A
XR_001745131.1:n.473+28975G>A
XR_001745132.1:n.473+28975G>A
NM_000905.4:c.269+803C>T MANE Select	NP_000896.1:n.269+803C>T