Canonical Allele Identifier: CA14096484
Gene: TRPM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.31026364C>T , CM000677.2:g.31026364C>T GRCh38
NC_000015.9:g.31318567C>T , CM000677.1:g.31318567C>T GRCh37
NC_000015.8:g.29105859C>T NCBI36
NG_016453.1:g.80358G>A
NG_016453.2:g.139910G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000711434.1:c.3449-93G>A ENSP00000518752.1:n.3449-93G>A
ENST00000397795.7:c.3431-93G>A ENSP00000380897.2:n.3431-93G>A
ENST00000558445.6:c.3548-93G>A ENSP00000452946.2:n.3548-93G>A
ENST00000559177.6:c.893-93G>A ENSP00000453477.2:n.893-93G>A
ENST00000256552.11:c.3497-93G>A MANE Select ENSP00000256552.7:n.3497-93G>A
ENST00000256552.10:c.3497-93G>A ENSP00000256552.6:n.3497-93G>A
ENST00000397795.6:c.3431-93G>A ENSP00000380897.2:n.3431-93G>A
ENST00000542188.5:c.3548-93G>A ENSP00000437849.1:n.3548-93G>A
ENST00000558445.5:c.3431-93G>A ENSP00000452946.1:n.3431-93G>A
ENST00000558768.5:c.3200-93G>A ENSP00000453119.2:n.3200-93G>A
ENST00000559177.5:c.776-93G>A ENSP00000453477.1:n.776-93G>A
ENST00000560801.5:c.3073-93G>A ENSP00000453644.2:n.3073-93G>A
NM_001252020.1:c.3548-93G>A NP_001238949.1:n.3548-93G>A
NM_001252024.1:c.3497-93G>A NP_001238953.1:n.3497-93G>A
NM_002420.5:c.3431-93G>A NP_002411.3:n.3431-93G>A
XR_932055.1:n.113+46C>T
XR_932057.1:n.113+46C>T
XR_001751769.1:n.131+46C>T
NM_001252024.2:c.3497-93G>A MANE Select NP_001238953.1:n.3497-93G>A
NM_002420.6:c.3431-93G>A NP_002411.3:n.3431-93G>A
NM_001252020.2:c.3548-93G>A NP_001238949.1:n.3548-93G>A