Canonical Allele Identifier: CA1505233673

Gene: NPY2R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155214881C= , CM000666.2:g.155214881C=	GRCh38
NC_000004.11:g.156136033C= , CM000666.1:g.156136033C=	GRCh37
NC_000004.10:g.156355483C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.942C= MANE Select	ENSP00000332591.3:p.Ala314=
ENST00000329476.3:c.942C=	ENSP00000332591.3:p.Ala314=
ENST00000506608.1:c.942C=	ENSP00000426366.1:p.Ala314=
NM_000910.3:c.942C=	NP_000901.1:p.Ala314=
XM_005263033.3:c.942C=	XP_005263090.1:p.Ala314=
XM_005263034.3:c.942C=	XP_005263091.1:p.Ala314=
XM_005263033.4:c.942C=	XP_005263090.1:p.Ala314=
XM_005263034.4:c.942C=	XP_005263091.1:p.Ala314=
NM_000910.4:c.942C= MANE Select	NP_000901.1:p.Ala314=
NM_001370180.1:c.942C=	NP_001357109.1:p.Ala314=
NM_001375470.1:c.942C=	NP_001362399.1:p.Ala314=