Canonical Allele Identifier: CA1151578883

Gene: TAS1R1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6571371C>G , CM000663.2:g.6571371C>G	GRCh38
NC_000001.10:g.6631431C>G , CM000663.1:g.6631431C>G	GRCh37
NC_000001.9:g.6554018C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333172.11:c.498+156C>G MANE Select	ENSP00000331867.6:n.498+156C>G
ENST00000328191.5:c.264+156C>G	ENSP00000327705.5:n.264+156C>G
ENST00000333172.10:c.498+156C>G	ENSP00000331867.6:n.498+156C>G
ENST00000351136.7:c.498+156C>G	ENSP00000312558.5:n.498+156C>G
ENST00000411823.5:c.275+156C>G
ENST00000415267.1:c.275+156C>G
NM_138697.3:c.498+156C>G	NP_619642.2:n.498+156C>G
NM_177540.2:c.498+156C>G	NP_803884.1:n.498+156C>G
XM_011542202.1:c.384+156C>G	XP_011540504.1:n.384+156C>G
XM_011542203.1:c.264+156C>G	XP_011540505.1:n.264+156C>G
XM_011542204.1:c.264+156C>G	XP_011540506.1:n.264+156C>G
XM_011542206.1:c.504+156C>G	XP_011540508.1:n.504+156C>G
XM_011542203.2:c.264+156C>G	XP_011540505.1:n.264+156C>G
XM_011542206.2:c.504+156C>G	XP_011540508.1:n.504+156C>G
XM_017002402.1:c.504+156C>G	XP_016857891.1:n.504+156C>G
XM_017002403.1:c.504+156C>G	XP_016857892.1:n.504+156C>G
XR_001737881.1:n.88-1388G>C
XR_002958250.1:n.88-1388G>C
NM_138697.4:c.498+156C>G MANE Select	NP_619642.2:n.498+156C>G
NM_177540.3:c.498+156C>G	NP_803884.1:n.498+156C>G