Canonical Allele Identifier: CA2016164473

Gene: TAS2R13 PRR4 PRH1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10908523T= , CM000674.2:g.10908523T=	GRCh38
NC_000012.11:g.11061122T= , CM000674.1:g.11061122T=	GRCh37
NC_000012.10:g.10952389T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_023920.2:c.776A= (TAS2R13) MANE Select	NP_076409.1:p.Asn259=
ENST00000390677.2:c.776A= (TAS2R13) MANE Select	ENSP00000375095.2:p.Asn259=
NM_001291314.1:c.-58-24248A= (PRH1)	NP_001278243.1:n.-58-24248A=
NM_001291314.2:c.-58-24248A= (PRH1)	NP_001278243.1:n.-58-24248A=
NM_001291315.1:c.104-25427A= (PRH1)	NP_001278244.1:n.104-25427A=
NM_001291315.2:c.104-25427A= (PRH1)	NP_001278244.1:n.104-25427A=
NR_037918.2:n.545-24248A=
ENST00000535024.5:c.104-60116A= (PRR4)	ENSP00000481571.1:n.104-60116A=
ENST00000535024.6:c.104-60116A=	ENSP00000481571.2:n.104-60116A=
ENST00000536086.2:n.90-16598A= (PRH1)
ENST00000536668.2:c.177-24248A=	ENSP00000482961.1:n.177-24248A=
ENST00000539853.5:c.-58-24248A= (PRH1)	ENSP00000482068.1:n.-58-24248A=
ENST00000541977.5:n.360-25427A= (PRH1)
ENST00000546317.1:n.53-13194A= (PRR4)
ENST00000703543.1:c.-58-24248A=	ENSP00000515364.1:n.-58-24248A=