Canonical Allele Identifier: CA373688296

Gene: TRPM6

Linked Data

• MyVariant Identifiers: chr9:g.77416920T>C (hg19) ; chr9:g.74802004T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74802004T>C , CM000671.2:g.74802004T>C	GRCh38
NC_000009.11:g.77416920T>C , CM000671.1:g.77416920T>C	GRCh37
NC_000009.10:g.76606740T>C	NCBI36
NG_017036.1:g.91091A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360774.6:c.1903A>G MANE Select	ENSP00000354006.1:p.Thr635Ala
ENST00000360774.5:c.1903A>G	ENSP00000354006.1:p.Thr635Ala
ENST00000361255.7:c.1888A>G	ENSP00000354962.3:p.Thr630Ala
ENST00000449912.6:c.1888A>G	ENSP00000396672.2:p.Thr630Ala
NM_001177310.1:c.1888A>G	NP_001170781.1:p.Thr630Ala
NM_001177311.1:c.1888A>G	NP_001170782.1:p.Thr630Ala
NM_017662.4:c.1903A>G	NP_060132.3:p.Thr635Ala
XM_011518244.1:c.1903A>G	XP_011516546.1:p.Thr635Ala
XM_011518245.1:c.1810A>G	XP_011516547.1:p.Thr604Ala
XM_011518246.1:c.1903A>G	XP_011516548.1:p.Thr635Ala
XM_011518247.1:c.1903A>G	XP_011516549.1:p.Thr635Ala
XM_011518248.1:c.1762A>G	XP_011516550.1:p.Thr588Ala
XM_011518249.1:c.1669A>G	XP_011516551.1:p.Thr557Ala
XM_011518250.1:c.1903A>G	XP_011516552.1:p.Thr635Ala
XM_011518251.1:c.1174A>G	XP_011516553.1:p.Thr392Ala
XM_011518252.1:c.1903A>G	XP_011516554.1:p.Thr635Ala
XM_011518254.1:c.1903A>G	XP_011516556.1:p.Thr635Ala
XM_011518255.1:c.1903A>G	XP_011516557.1:p.Thr635Ala
XR_929716.1:n.2141A>G
XR_929717.1:n.2141A>G
XR_929718.1:n.2141A>G
XM_011518251.2:c.1174A>G	XP_011516553.1:p.Thr392Ala
XM_011518252.2:c.1903A>G	XP_011516554.1:p.Thr635Ala
XM_011518255.2:c.1903A>G	XP_011516557.1:p.Thr635Ala
XM_017014287.1:c.1669A>G	XP_016869776.1:p.Thr557Ala
XM_017014288.1:c.1669A>G	XP_016869777.1:p.Thr557Ala
XM_017014289.1:c.1903A>G	XP_016869778.1:p.Thr635Ala
XR_001746185.1:n.2141A>G
XR_929717.2:n.2141A>G
NM_017662.5:c.1903A>G MANE Select	NP_060132.3:p.Thr635Ala
NM_001177310.2:c.1888A>G	NP_001170781.1:p.Thr630Ala
NM_001177311.2:c.1888A>G	NP_001170782.1:p.Thr630Ala