Canonical Allele Identifier: CA367051762

Gene: NPY

Linked Data

• MyVariant Identifiers: chr7:g.24324918T>G (hg19) ; chr7:g.24285299T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285299T>G , CM000669.2:g.24285299T>G	GRCh38
NC_000007.13:g.24324918T>G , CM000669.1:g.24324918T>G	GRCh37
NC_000007.12:g.24291443T>G	NCBI36
NG_016148.1:g.6112T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.59T>G MANE Select	ENSP00000242152.2:p.Val20Gly
ENST00000242152.6:c.59T>G	ENSP00000242152.2:p.Val20Gly
ENST00000405982.1:c.59T>G	ENSP00000385282.1:p.Val20Gly
ENST00000407573.5:c.59T>G	ENSP00000384364.1:p.Val20Gly
NM_000905.3:c.59T>G	NP_000896.1:p.Val20Gly
XM_017012910.1:c.42-29600A>C	XP_016868399.1:n.42-29600A>C
XM_017012911.1:c.42-29600A>C	XP_016868400.1:n.42-29600A>C
XR_001745121.1:n.473+34058A>C
XR_001745122.1:n.345-88270A>C
XR_001745123.1:n.473+34058A>C
XR_001745124.1:n.473+34058A>C
XR_001745125.1:n.473+34058A>C
XR_001745126.1:n.473+34058A>C
XR_001745127.1:n.345-29600A>C
XR_001745129.1:n.473+34058A>C
XR_001745130.1:n.473+34058A>C
XR_001745131.1:n.473+34058A>C
XR_001745132.1:n.473+34058A>C
NM_000905.4:c.59T>G MANE Select	NP_000896.1:p.Val20Gly