Canonical Allele Identifier: CA2682048916

Gene: NPY

Linked Data

• gnomAD v4: 7-24291834-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291834T>G , CM000669.2:g.24291834T>G	GRCh38
NC_000007.13:g.24331453T>G , CM000669.1:g.24331453T>G	GRCh37
NC_000007.12:g.24297978T>G	NCBI36
NG_016148.1:g.12647T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*147T>G MANE Select	ENSP00000242152.2:n.*147T>G
ENST00000242152.6:c.*147T>G	ENSP00000242152.2:n.*147T>G
NM_000905.3:c.*147T>G	NP_000896.1:n.*147T>G
XM_017012910.1:c.41+27523A>C	XP_016868399.1:n.41+27523A>C
XM_017012911.1:c.41+27523A>C	XP_016868400.1:n.41+27523A>C
XR_001745121.1:n.473+27523A>C
XR_001745122.1:n.345-94805A>C
XR_001745123.1:n.473+27523A>C
XR_001745124.1:n.473+27523A>C
XR_001745125.1:n.473+27523A>C
XR_001745126.1:n.473+27523A>C
XR_001745127.1:n.345-36135A>C
XR_001745129.1:n.473+27523A>C
XR_001745130.1:n.473+27523A>C
XR_001745131.1:n.473+27523A>C
XR_001745132.1:n.473+27523A>C
NM_000905.4:c.*147T>G MANE Select	NP_000896.1:n.*147T>G