Canonical Allele Identifier: CA2682048162

Gene: NPY

Linked Data

• gnomAD v4: 7-24285140-T-TCGCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285140_24285141insCGCGG , CM000669.2:g.24285140_24285141insCGCGG	GRCh38
NC_000007.13:g.24324759_24324760insCGCGG , CM000669.1:g.24324759_24324760insCGCGG	GRCh37
NC_000007.12:g.24291284_24291285insCGCGG	NCBI36
NG_016148.1:g.5953_5954insCGCGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-101_1-100insCGCGG MANE Select	ENSP00000242152.2:n.1-101_1-100insCGCGG
ENST00000242152.6:c.1-101_1-100insCGCGG	ENSP00000242152.2:n.1-101_1-100insCGCGG
ENST00000405982.1:c.-101_-100insCGCGG	ENSP00000385282.1:n.-101_-100insCGCGG
ENST00000407573.5:c.-1+64_-1+65insCGCGG	ENSP00000384364.1:n.-1+64_-1+65insCGCGG
NM_000905.3:c.1-101_1-100insCGCGG	NP_000896.1:n.1-101_1-100insCGCGG
XM_017012910.1:c.42-29442_42-29441insCCGCG	XP_016868399.1:n.42-29442_42-29441insCCGCG
XM_017012911.1:c.42-29442_42-29441insCCGCG	XP_016868400.1:n.42-29442_42-29441insCCGCG
XR_001745121.1:n.473+34216_473+34217insCCGCG
XR_001745122.1:n.345-88112_345-88111insCCGCG
XR_001745123.1:n.473+34216_473+34217insCCGCG
XR_001745124.1:n.473+34216_473+34217insCCGCG
XR_001745125.1:n.473+34216_473+34217insCCGCG
XR_001745126.1:n.473+34216_473+34217insCCGCG
XR_001745127.1:n.345-29442_345-29441insCCGCG
XR_001745129.1:n.473+34216_473+34217insCCGCG
XR_001745130.1:n.473+34216_473+34217insCCGCG
XR_001745131.1:n.473+34216_473+34217insCCGCG
XR_001745132.1:n.473+34216_473+34217insCCGCG
NM_000905.4:c.1-101_1-100insCGCGG MANE Select	NP_000896.1:n.1-101_1-100insCGCGG