Canonical Allele Identifier: CA155829778
Gene: NPY HGNC NCBI

Linked Data

dbSNP Id: rs16128
MyVariant Identifiers: chr7:g.24331044C>A (hg19) chr7:g.24291425C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24291425C>A , CM000669.2:g.24291425C>A GRCh38
NC_000007.13:g.24331044C>A , CM000669.1:g.24331044C>A GRCh37
NC_000007.12:g.24297569C>A NCBI36
NG_016148.1:g.12238C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.270-238C>A MANE Select ENSP00000242152.2:n.270-238C>A
ENST00000242152.6:c.270-238C>A ENSP00000242152.2:n.270-238C>A
ENST00000405982.1:c.270-238C>A ENSP00000385282.1:n.270-238C>A
ENST00000407573.5:c.270-238C>A ENSP00000384364.1:n.270-238C>A
NM_000905.3:c.270-238C>A NP_000896.1:n.270-238C>A
XM_017012910.1:c.41+27932G>T XP_016868399.1:n.41+27932G>T
XM_017012911.1:c.41+27932G>T XP_016868400.1:n.41+27932G>T
XR_001745121.1:n.473+27932G>T
XR_001745122.1:n.345-94396G>T
XR_001745123.1:n.473+27932G>T
XR_001745124.1:n.473+27932G>T
XR_001745125.1:n.473+27932G>T
XR_001745126.1:n.473+27932G>T
XR_001745127.1:n.345-35726G>T
XR_001745129.1:n.473+27932G>T
XR_001745130.1:n.473+27932G>T
XR_001745131.1:n.473+27932G>T
XR_001745132.1:n.473+27932G>T
NM_000905.4:c.270-238C>A MANE Select NP_000896.1:n.270-238C>A
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