Canonical Allele Identifier: CA373670608

Gene: TRPM6

Linked Data

• MyVariant Identifiers: chr9:g.77397318G>C (hg19) ; chr9:g.74782402G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74782402G>C , CM000671.2:g.74782402G>C	GRCh38
NC_000009.11:g.77397318G>C , CM000671.1:g.77397318G>C	GRCh37
NC_000009.10:g.76587138G>C	NCBI36
NG_017036.1:g.110693C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360774.6:c.3169C>G MANE Select	ENSP00000354006.1:p.Gln1057Glu
ENST00000360774.5:c.3169C>G	ENSP00000354006.1:p.Gln1057Glu
ENST00000361255.7:c.3154C>G	ENSP00000354962.3:p.Gln1052Glu
ENST00000449912.6:c.3154C>G	ENSP00000396672.2:p.Gln1052Glu
NM_001177310.1:c.3154C>G	NP_001170781.1:p.Gln1052Glu
NM_001177311.1:c.3154C>G	NP_001170782.1:p.Gln1052Glu
NM_017662.4:c.3169C>G	NP_060132.3:p.Gln1057Glu
XM_011518244.1:c.3169C>G	XP_011516546.1:p.Gln1057Glu
XM_011518245.1:c.3076C>G	XP_011516547.1:p.Gln1026Glu
XM_011518246.1:c.3169C>G	XP_011516548.1:p.Gln1057Glu
XM_011518247.1:c.3040C>G	XP_011516549.1:p.Gln1014Glu
XM_011518248.1:c.3028C>G	XP_011516550.1:p.Gln1010Glu
XM_011518249.1:c.2935C>G	XP_011516551.1:p.Gln979Glu
XM_011518250.1:c.2893C>G	XP_011516552.1:p.Gln965Glu
XM_011518251.1:c.2440C>G	XP_011516553.1:p.Gln814Glu
XM_011518252.1:c.3169C>G	XP_011516554.1:p.Gln1057Glu
XM_011518253.1:c.1102C>G	XP_011516555.1:p.Gln368Glu
XM_011518254.1:c.3169C>G	XP_011516556.1:p.Gln1057Glu
XM_011518255.1:c.3169C>G	XP_011516557.1:p.Gln1057Glu
XR_929716.1:n.3407C>G
XR_929717.1:n.3407C>G
XR_929718.1:n.3332+277C>G
XM_011518251.2:c.2440C>G	XP_011516553.1:p.Gln814Glu
XM_011518252.2:c.3169C>G	XP_011516554.1:p.Gln1057Glu
XM_011518255.2:c.3169C>G	XP_011516557.1:p.Gln1057Glu
XM_017014287.1:c.2806C>G	XP_016869776.1:p.Gln936Glu
XM_017014288.1:c.2659C>G	XP_016869777.1:p.Gln887Glu
XM_017014289.1:c.3169C>G	XP_016869778.1:p.Gln1057Glu
XR_001746185.1:n.3407C>G
XR_929717.2:n.3407C>G
NM_017662.5:c.3169C>G MANE Select	NP_060132.3:p.Gln1057Glu
NM_001177310.2:c.3154C>G	NP_001170781.1:p.Gln1052Glu
NM_001177311.2:c.3154C>G	NP_001170782.1:p.Gln1052Glu