Canonical Allele Identifier: CA1335979591
Gene: TRPM8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233945826C= , CM000664.2:g.233945826C= GRCh38
NC_000002.11:g.234854470C= , CM000664.1:g.234854470C= GRCh37
NC_000002.10:g.234519209C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000324695.9:c.700-30C= MANE Select ENSP00000323926.4:n.700-30C=
ENST00000324695.8:c.700-30C= ENSP00000323926.4:n.700-30C=
ENST00000433712.6:c.-24-30C= ENSP00000404423.3:n.-24-30C=
ENST00000444298.5:c.700-30C= ENSP00000396745.1:n.700-30C=
NM_024080.4:c.700-30C= NP_076985.4:n.700-30C=
XM_011511810.1:c.700-30C= XP_011510112.1:n.700-30C=
XM_011511810.2:c.700-30C= XP_011510112.1:n.700-30C=
XM_017004891.1:c.469-30C= XP_016860380.1:n.469-30C=
XM_024453132.1:c.469-30C= XP_024308900.1:n.469-30C=
NM_024080.5:c.700-30C= MANE Select NP_076985.4:n.700-30C=
NM_001397606.1:c.700-30C= NP_001384535.1:n.700-30C=
NM_001397607.1:c.550-30C= NP_001384536.1:n.550-30C=
NM_001397608.1:c.700-30C= NP_001384537.1:n.700-30C=
NM_001397609.1:c.469-30C= NP_001384538.1:n.469-30C=
NM_001397610.1:c.469-30C= NP_001384539.1:n.469-30C=
NM_001397611.1:c.469-30C= NP_001384540.1:n.469-30C=
NM_001397612.1:c.469-30C= NP_001384541.1:n.469-30C=
NM_001397613.1:c.469-30C= NP_001384542.1:n.469-30C=
NM_001397615.1:c.-311-1262C= NP_001384544.1:n.-311-1262C=
NM_001397635.1:c.29-1262C= NP_001384564.1:n.29-1262C=