Canonical Allele Identifier: CA1948149219
Gene: TRPM5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2422886C= , CM000673.2:g.2422886C= GRCh38
NC_000011.9:g.2444116C= , CM000673.1:g.2444116C= GRCh37
NC_000011.8:g.2400692C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696290.1:c.117+34G= MANE Select ENSP00000512529.1:n.117+34G=
ENST00000155858.10:c.117+34G= ENSP00000155858.5:n.117+34G=
ENST00000528453.1:c.117+34G= ENSP00000436809.1:n.117+34G=
ENST00000533060.5:c.117+34G= ENSP00000434121.1:n.117+34G=
ENST00000533881.5:c.93+34G= ENSP00000434383.1:n.93+34G=
NM_014555.3:c.117+34G= NP_055370.1:n.117+34G=
XM_011520035.1:c.378+34G= XP_011518337.1:n.378+34G=
XM_017017628.1:c.171+34G= XP_016873117.1:n.171+34G=
NM_014555.4:c.117+34G= MANE Select NP_055370.1:n.117+34G=
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