Canonical Allele Identifier: CA1948131329
Gene: TRPM5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2411552G= , CM000673.2:g.2411552G= GRCh38
NC_000011.9:g.2432782G= , CM000673.1:g.2432782G= GRCh37
NC_000011.8:g.2389358G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696290.1:c.2608-26C= MANE Select ENSP00000512529.1:n.2608-26C=
ENST00000155858.10:c.2608-26C= ENSP00000155858.5:n.2608-26C=
ENST00000528453.1:c.2608-26C= ENSP00000436809.1:n.2608-26C=
ENST00000533060.5:c.2608-26C= ENSP00000434121.1:n.2608-26C=
ENST00000533881.5:c.2590-26C= ENSP00000434383.1:n.2590-26C=
NM_014555.3:c.2608-26C= NP_055370.1:n.2608-26C=
XM_011520035.1:c.2869-26C= XP_011518337.1:n.2869-26C=
XM_017017628.1:c.2662-26C= XP_016873117.1:n.2662-26C=
NM_014555.4:c.2608-26C= MANE Select NP_055370.1:n.2608-26C=