Canonical Allele Identifier: CA5084200

Gene: TRPM6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74762808C>T , CM000671.2:g.74762808C>T	GRCh38
NC_000009.11:g.77377724C>T , CM000671.1:g.77377724C>T	GRCh37
NC_000009.10:g.76567544C>T	NCBI36
NG_017036.1:g.130287G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_017662.5:c.3863G>A MANE Select	NP_060132.3:p.Gly1288Glu
ENST00000360774.6:c.3863G>A MANE Select	ENSP00000354006.1:p.Gly1288Glu
NM_001177310.1:c.3848G>A	NP_001170781.1:p.Gly1283Glu
NM_001177310.2:c.3848G>A	NP_001170781.1:p.Gly1283Glu
NM_001177311.1:c.3848G>A	NP_001170782.1:p.Gly1283Glu
NM_001177311.2:c.3848G>A	NP_001170782.1:p.Gly1283Glu
NM_017662.4:c.3863G>A	NP_060132.3:p.Gly1288Glu
ENST00000360774.5:c.3863G>A	ENSP00000354006.1:p.Gly1288Glu
ENST00000361255.7:c.3848G>A	ENSP00000354962.3:p.Gly1283Glu
ENST00000449912.6:c.3848G>A	ENSP00000396672.2:p.Gly1283Glu
XM_011518244.1:c.3863G>A	XP_011516546.1:p.Gly1288Glu
XM_011518245.1:c.3770G>A	XP_011516547.1:p.Gly1257Glu
XM_011518246.1:c.3863G>A	XP_011516548.1:p.Gly1288Glu
XM_011518247.1:c.3734G>A	XP_011516549.1:p.Gly1245Glu
XM_011518248.1:c.3722G>A	XP_011516550.1:p.Gly1241Glu
XM_011518249.1:c.3629G>A	XP_011516551.1:p.Gly1210Glu
XM_011518250.1:c.3587G>A	XP_011516552.1:p.Gly1196Glu
XM_011518251.1:c.3134G>A	XP_011516553.1:p.Gly1045Glu
XM_011518251.2:c.3134G>A	XP_011516553.1:p.Gly1045Glu
XM_011518252.1:c.3863G>A	XP_011516554.1:p.Gly1288Glu
XM_011518252.2:c.3863G>A	XP_011516554.1:p.Gly1288Glu
XM_011518253.1:c.1796G>A	XP_011516555.1:p.Gly599Glu
XM_017014287.1:c.3500G>A	XP_016869776.1:p.Gly1167Glu
XM_017014288.1:c.3353G>A	XP_016869777.1:p.Gly1118Glu
XM_017014289.1:c.3863G>A	XP_016869778.1:p.Gly1288Glu
XR_001746185.1:n.4101G>A
XR_929716.1:n.4101G>A
XR_929717.1:n.4101G>A
XR_929717.2:n.4101G>A