Canonical Allele Identifier: CA454131859

Gene: NPY

Linked Data

• MyVariant Identifiers: chr7:g.24324916C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285297C>G , CM000669.2:g.24285297C>G	GRCh38
NC_000007.13:g.24324916C>G , CM000669.1:g.24324916C>G	GRCh37
NC_000007.12:g.24291441C>G	NCBI36
NG_016148.1:g.6110C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.57C>G MANE Select	ENSP00000242152.2:p.Leu19=
ENST00000242152.6:c.57C>G	ENSP00000242152.2:p.Leu19=
ENST00000405982.1:c.57C>G	ENSP00000385282.1:p.Leu19=
ENST00000407573.5:c.57C>G	ENSP00000384364.1:p.Leu19=
NM_000905.3:c.57C>G	NP_000896.1:p.Leu19=
XM_017012910.1:c.42-29598G>C	XP_016868399.1:n.42-29598G>C
XM_017012911.1:c.42-29598G>C	XP_016868400.1:n.42-29598G>C
XR_001745121.1:n.473+34060G>C
XR_001745122.1:n.345-88268G>C
XR_001745123.1:n.473+34060G>C
XR_001745124.1:n.473+34060G>C
XR_001745125.1:n.473+34060G>C
XR_001745126.1:n.473+34060G>C
XR_001745127.1:n.345-29598G>C
XR_001745129.1:n.473+34060G>C
XR_001745130.1:n.473+34060G>C
XR_001745131.1:n.473+34060G>C
XR_001745132.1:n.473+34060G>C
NM_000905.4:c.57C>G MANE Select	NP_000896.1:p.Leu19=