Canonical Allele Identifier: CA1694877498

Gene: NPY

Linked Data

• dbSNP Id: rs1787631035
• gnomAD v4: 7-24291861-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291861A>C , CM000669.2:g.24291861A>C	GRCh38
NC_000007.13:g.24331480A>C , CM000669.1:g.24331480A>C	GRCh37
NC_000007.12:g.24298005A>C	NCBI36
NG_016148.1:g.12674A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*174A>C MANE Select	ENSP00000242152.2:n.*174A>C
ENST00000242152.6:c.*174A>C	ENSP00000242152.2:n.*174A>C
NM_000905.3:c.*174A>C	NP_000896.1:n.*174A>C
XM_017012910.1:c.41+27496T>G	XP_016868399.1:n.41+27496T>G
XM_017012911.1:c.41+27496T>G	XP_016868400.1:n.41+27496T>G
XR_001745121.1:n.473+27496T>G
XR_001745122.1:n.345-94832T>G
XR_001745123.1:n.473+27496T>G
XR_001745124.1:n.473+27496T>G
XR_001745125.1:n.473+27496T>G
XR_001745126.1:n.473+27496T>G
XR_001745127.1:n.345-36162T>G
XR_001745129.1:n.473+27496T>G
XR_001745130.1:n.473+27496T>G
XR_001745131.1:n.473+27496T>G
XR_001745132.1:n.473+27496T>G
NM_000905.4:c.*174A>C MANE Select	NP_000896.1:n.*174A>C