Canonical Allele Identifier: CA12500636
Gene: NPY HGNC NCBI

Linked Data

dbSNP Id: rs16140

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24285189C>G , CM000669.2:g.24285189C>G GRCh38
NC_000007.13:g.24324808C>G , CM000669.1:g.24324808C>G GRCh37
NC_000007.12:g.24291333C>G NCBI36
NG_016148.1:g.6002C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.1-52C>G MANE Select ENSP00000242152.2:n.1-52C>G
ENST00000242152.6:c.1-52C>G ENSP00000242152.2:n.1-52C>G
ENST00000405982.1:c.-52C>G ENSP00000385282.1:n.-52C>G
ENST00000407573.5:c.1-52C>G ENSP00000384364.1:n.1-52C>G
NM_000905.3:c.1-52C>G NP_000896.1:n.1-52C>G
XM_017012910.1:c.42-29490G>C XP_016868399.1:n.42-29490G>C
XM_017012911.1:c.42-29490G>C XP_016868400.1:n.42-29490G>C
XR_001745121.1:n.473+34168G>C
XR_001745122.1:n.345-88160G>C
XR_001745123.1:n.473+34168G>C
XR_001745124.1:n.473+34168G>C
XR_001745125.1:n.473+34168G>C
XR_001745126.1:n.473+34168G>C
XR_001745127.1:n.345-29490G>C
XR_001745129.1:n.473+34168G>C
XR_001745130.1:n.473+34168G>C
XR_001745131.1:n.473+34168G>C
XR_001745132.1:n.473+34168G>C
NM_000905.4:c.1-52C>G MANE Select NP_000896.1:n.1-52C>G