Canonical Allele Identifier: CA351098305

Gene: TRPM8

Linked Data

• MyVariant Identifiers: chr2:g.234854500G>T (hg19) ; chr2:g.233945856G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233945856G>T , CM000664.2:g.233945856G>T	GRCh38
NC_000002.11:g.234854500G>T , CM000664.1:g.234854500G>T	GRCh37
NC_000002.10:g.234519239G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324695.9:c.700G>T MANE Select	ENSP00000323926.4:p.Gly234Cys
ENST00000324695.8:c.700G>T	ENSP00000323926.4:p.Gly234Cys
ENST00000433712.6:c.-24G>T	ENSP00000404423.3:n.-24G>T
ENST00000444298.5:c.700G>T	ENSP00000396745.1:p.Gly234Cys
NM_024080.4:c.700G>T	NP_076985.4:p.Gly234Cys
XM_011511810.1:c.700G>T	XP_011510112.1:p.Gly234Cys
XM_011511810.2:c.700G>T	XP_011510112.1:p.Gly234Cys
XM_017004891.1:c.469G>T	XP_016860380.1:p.Gly157Cys
XM_024453132.1:c.469G>T	XP_024308900.1:p.Gly157Cys
NM_024080.5:c.700G>T MANE Select	NP_076985.4:p.Gly234Cys
NM_001397606.1:c.700G>T	NP_001384535.1:p.Gly234Cys
NM_001397607.1:c.550G>T	NP_001384536.1:p.Gly184Cys
NM_001397608.1:c.700G>T	NP_001384537.1:p.Gly234Cys
NM_001397609.1:c.469G>T	NP_001384538.1:p.Gly157Cys
NM_001397610.1:c.469G>T	NP_001384539.1:p.Gly157Cys
NM_001397611.1:c.469G>T	NP_001384540.1:p.Gly157Cys
NM_001397612.1:c.469G>T	NP_001384541.1:p.Gly157Cys
NM_001397613.1:c.469G>T	NP_001384542.1:p.Gly157Cys
NM_001397615.1:c.-311-1232G>T	NP_001384544.1:n.-311-1232G>T
NM_001397635.1:c.29-1232G>T	NP_001384564.1:n.29-1232G>T