Canonical Allele Identifier: CA358668418

Gene: NPY1R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163325897A>G , CM000666.2:g.163325897A>G	GRCh38
NC_000004.11:g.164247049A>G , CM000666.1:g.164247049A>G	GRCh37
NC_000004.10:g.164466499A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000909.6:c.658T>C MANE Select	NP_000900.1:p.Tyr220His
ENST00000296533.3:c.658T>C MANE Select	ENSP00000354652.2:p.Tyr220His
NM_000909.5:c.658T>C	NP_000900.1:p.Tyr220His
ENST00000296533.2:c.658T>C	ENSP00000354652.2:p.Tyr220His
ENST00000504391.5:c.-72T>C	ENSP00000422963.1:n.-72T>C
ENST00000509586.5:c.-72T>C	ENSP00000427284.1:n.-72T>C
ENST00000512819.1:c.124T>C	ENSP00000421618.1:p.Tyr42His
XM_005263031.2:c.658T>C	XP_005263088.1:p.Tyr220His
XM_005263031.4:c.658T>C	XP_005263088.1:p.Tyr220His
XM_011532010.1:c.658T>C	XP_011530312.1:p.Tyr220His
XM_011532010.3:c.658T>C	XP_011530312.1:p.Tyr220His