Canonical Allele Identifier: CA13476334

Gene: TRPM5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2409635C>T , CM000673.2:g.2409635C>T	GRCh38
NC_000011.9:g.2430865C>T , CM000673.1:g.2430865C>T	GRCh37
NC_000011.8:g.2387441C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696290.1:c.2782+1717G>A MANE Select	ENSP00000512529.1:n.2782+1717G>A
ENST00000155858.10:c.2782+1717G>A	ENSP00000155858.5:n.2782+1717G>A
ENST00000528453.1:c.2782+1717G>A	ENSP00000436809.1:n.2782+1717G>A
ENST00000533060.5:c.2782+1717G>A	ENSP00000434121.1:n.2782+1717G>A
ENST00000533881.5:c.2764+1717G>A	ENSP00000434383.1:n.2764+1717G>A
NM_014555.3:c.2782+1717G>A	NP_055370.1:n.2782+1717G>A
XM_011520035.1:c.3043+1717G>A	XP_011518337.1:n.3043+1717G>A
XM_017017628.1:c.2836+1717G>A	XP_016873117.1:n.2836+1717G>A
NM_014555.4:c.2782+1717G>A MANE Select	NP_055370.1:n.2782+1717G>A