Canonical Allele Identifier: CA2526611046

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285001T>C , CM000669.2:g.24285001T>C	GRCh38
NC_000007.13:g.24324620T>C , CM000669.1:g.24324620T>C	GRCh37
NC_000007.12:g.24291145T>C	NCBI36
NG_016148.1:g.5814T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-240T>C MANE Select	ENSP00000242152.2:n.1-240T>C
ENST00000242152.6:c.1-240T>C	ENSP00000242152.2:n.1-240T>C
ENST00000407573.5:c.-76T>C	ENSP00000384364.1:n.-76T>C
NM_000905.3:c.1-240T>C	NP_000896.1:n.1-240T>C
XM_017012910.1:c.42-29302A>G	XP_016868399.1:n.42-29302A>G
XM_017012911.1:c.42-29302A>G	XP_016868400.1:n.42-29302A>G
XR_001745121.1:n.473+34356A>G
XR_001745122.1:n.345-87972A>G
XR_001745123.1:n.473+34356A>G
XR_001745124.1:n.473+34356A>G
XR_001745125.1:n.473+34356A>G
XR_001745126.1:n.473+34356A>G
XR_001745127.1:n.345-29302A>G
XR_001745129.1:n.473+34356A>G
XR_001745130.1:n.473+34356A>G
XR_001745131.1:n.473+34356A>G
XR_001745132.1:n.473+34356A>G
NM_000905.4:c.1-240T>C MANE Select	NP_000896.1:n.1-240T>C