Canonical Allele Identifier: CA110082142

Gene: NPY1R

Linked Data

• dbSNP Id: rs968642804
• MyVariant Identifiers: chr4:g.164245855_164245858del (hg19) ; chr4:g.163324703_163324706del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324705_163324708del , CM000666.2:g.163324705_163324708del	GRCh38
NC_000004.11:g.164245857_164245860del , CM000666.1:g.164245857_164245860del	GRCh37
NC_000004.10:g.164465307_164465310del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296533.3:c.*597_*600del MANE Select	ENSP00000354652.2:n.*597_*600del
ENST00000296533.2:c.*597_*600del	ENSP00000354652.2:n.*597_*600del
NM_000909.5:c.*597_*600del	NP_000900.1:n.*597_*600del
XM_005263031.2:c.*597_*600del	XP_005263088.1:n.*597_*600del
XM_011532010.1:c.*597_*600del	XP_011530312.1:n.*597_*600del
XM_005263031.4:c.*597_*600del	XP_005263088.1:n.*597_*600del
XM_011532010.3:c.*597_*600del	XP_011530312.1:n.*597_*600del
NM_000909.6:c.*597_*600del MANE Select	NP_000900.1:n.*597_*600del