Canonical Allele Identifier: CA1335966304

Gene: TRPM8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233919016G= , CM000664.2:g.233919016G=	GRCh38
NC_000002.11:g.234827661G= , CM000664.1:g.234827661G=	GRCh37
NC_000002.10:g.234492400G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024080.5:c.-6+1584G= MANE Select	NP_076985.4:n.-6+1584G=
ENST00000324695.9:c.-6+1584G= MANE Select	ENSP00000323926.4:n.-6+1584G=
NM_001397606.1:c.-6+1584G=	NP_001384535.1:n.-6+1584G=
NM_001397608.1:c.-6+1584G=	NP_001384537.1:n.-6+1584G=
NM_001397626.1:c.-6+1584G=	NP_001384555.1:n.-6+1584G=
NM_024080.4:c.-6+1584G=	NP_076985.4:n.-6+1584G=
ENST00000324695.8:c.-6+1584G=	ENSP00000323926.4:n.-6+1584G=
ENST00000433712.6:c.-729+1584G=	ENSP00000404423.3:n.-729+1584G=
ENST00000444298.5:c.-6+1584G=	ENSP00000396745.1:n.-6+1584G=
XM_011511810.1:c.-6+1584G=	XP_011510112.1:n.-6+1584G=
XM_011511810.2:c.-6+1584G=	XP_011510112.1:n.-6+1584G=