Canonical Allele Identifier: CA465505268

Gene: TRPM6

Linked Data

• dbSNP Id: rs1827494679
• gnomAD v3: 9-74782400-T-C
• gnomAD v4: 9-74782400-T-C
• MyVariant Identifiers: chr9:g.77397316T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74782400T>C , CM000671.2:g.74782400T>C	GRCh38
NC_000009.11:g.77397316T>C , CM000671.1:g.77397316T>C	GRCh37
NC_000009.10:g.76587136T>C	NCBI36
NG_017036.1:g.110695A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360774.6:c.3171A>G MANE Select	ENSP00000354006.1:p.Gln1057=
ENST00000360774.5:c.3171A>G	ENSP00000354006.1:p.Gln1057=
ENST00000361255.7:c.3156A>G	ENSP00000354962.3:p.Gln1052=
ENST00000449912.6:c.3156A>G	ENSP00000396672.2:p.Gln1052=
NM_001177310.1:c.3156A>G	NP_001170781.1:p.Gln1052=
NM_001177311.1:c.3156A>G	NP_001170782.1:p.Gln1052=
NM_017662.4:c.3171A>G	NP_060132.3:p.Gln1057=
XM_011518244.1:c.3171A>G	XP_011516546.1:p.Gln1057=
XM_011518245.1:c.3078A>G	XP_011516547.1:p.Gln1026=
XM_011518246.1:c.3171A>G	XP_011516548.1:p.Gln1057=
XM_011518247.1:c.3042A>G	XP_011516549.1:p.Gln1014=
XM_011518248.1:c.3030A>G	XP_011516550.1:p.Gln1010=
XM_011518249.1:c.2937A>G	XP_011516551.1:p.Gln979=
XM_011518250.1:c.2895A>G	XP_011516552.1:p.Gln965=
XM_011518251.1:c.2442A>G	XP_011516553.1:p.Gln814=
XM_011518252.1:c.3171A>G	XP_011516554.1:p.Gln1057=
XM_011518253.1:c.1104A>G	XP_011516555.1:p.Gln368=
XM_011518254.1:c.3171A>G	XP_011516556.1:p.Gln1057=
XM_011518255.1:c.3171A>G	XP_011516557.1:p.Gln1057=
XR_929716.1:n.3409A>G
XR_929717.1:n.3409A>G
XR_929718.1:n.3332+279A>G
XM_011518251.2:c.2442A>G	XP_011516553.1:p.Gln814=
XM_011518252.2:c.3171A>G	XP_011516554.1:p.Gln1057=
XM_011518255.2:c.3171A>G	XP_011516557.1:p.Gln1057=
XM_017014287.1:c.2808A>G	XP_016869776.1:p.Gln936=
XM_017014288.1:c.2661A>G	XP_016869777.1:p.Gln887=
XM_017014289.1:c.3171A>G	XP_016869778.1:p.Gln1057=
XR_001746185.1:n.3409A>G
XR_929717.2:n.3409A>G
NM_017662.5:c.3171A>G MANE Select	NP_060132.3:p.Gln1057=
NM_001177310.2:c.3156A>G	NP_001170781.1:p.Gln1052=
NM_001177311.2:c.3156A>G	NP_001170782.1:p.Gln1052=