Canonical Allele Identifier: CA1335979585
Gene: TRPM8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233945816A= , CM000664.2:g.233945816A= GRCh38
NC_000002.11:g.234854460A= , CM000664.1:g.234854460A= GRCh37
NC_000002.10:g.234519199A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000324695.9:c.700-40A= MANE Select ENSP00000323926.4:n.700-40A=
ENST00000324695.8:c.700-40A= ENSP00000323926.4:n.700-40A=
ENST00000433712.6:c.-24-40A= ENSP00000404423.3:n.-24-40A=
ENST00000444298.5:c.700-40A= ENSP00000396745.1:n.700-40A=
NM_024080.4:c.700-40A= NP_076985.4:n.700-40A=
XM_011511810.1:c.700-40A= XP_011510112.1:n.700-40A=
XM_011511810.2:c.700-40A= XP_011510112.1:n.700-40A=
XM_017004891.1:c.469-40A= XP_016860380.1:n.469-40A=
XM_024453132.1:c.469-40A= XP_024308900.1:n.469-40A=
NM_024080.5:c.700-40A= MANE Select NP_076985.4:n.700-40A=
NM_001397606.1:c.700-40A= NP_001384535.1:n.700-40A=
NM_001397607.1:c.550-40A= NP_001384536.1:n.550-40A=
NM_001397608.1:c.700-40A= NP_001384537.1:n.700-40A=
NM_001397609.1:c.469-40A= NP_001384538.1:n.469-40A=
NM_001397610.1:c.469-40A= NP_001384539.1:n.469-40A=
NM_001397611.1:c.469-40A= NP_001384540.1:n.469-40A=
NM_001397612.1:c.469-40A= NP_001384541.1:n.469-40A=
NM_001397613.1:c.469-40A= NP_001384542.1:n.469-40A=
NM_001397615.1:c.-311-1272A= NP_001384544.1:n.-311-1272A=
NM_001397635.1:c.29-1272A= NP_001384564.1:n.29-1272A=