Canonical Allele Identifier: CA194289366

Gene: TRPM6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74761783C>A , CM000671.2:g.74761783C>A	GRCh38
NC_000009.11:g.77376699C>A , CM000671.1:g.77376699C>A	GRCh37
NC_000009.10:g.76566519C>A	NCBI36
NG_017036.1:g.131312G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_017662.5:c.4698G>T MANE Select	NP_060132.3:p.Gly1566=
ENST00000360774.6:c.4698G>T MANE Select	ENSP00000354006.1:p.Gly1566=
NM_001177310.1:c.4683G>T	NP_001170781.1:p.Gly1561=
NM_001177310.2:c.4683G>T	NP_001170781.1:p.Gly1561=
NM_001177311.1:c.4683G>T	NP_001170782.1:p.Gly1561=
NM_001177311.2:c.4683G>T	NP_001170782.1:p.Gly1561=
NM_017662.4:c.4698G>T	NP_060132.3:p.Gly1566=
ENST00000360774.5:c.4698G>T	ENSP00000354006.1:p.Gly1566=
ENST00000361255.7:c.4683G>T	ENSP00000354962.3:p.Gly1561=
ENST00000449912.6:c.4683G>T	ENSP00000396672.2:p.Gly1561=
XM_011518244.1:c.4698G>T	XP_011516546.1:p.Gly1566=
XM_011518245.1:c.4605G>T	XP_011516547.1:p.Gly1535=
XM_011518246.1:c.4698G>T	XP_011516548.1:p.Gly1566=
XM_011518247.1:c.4569G>T	XP_011516549.1:p.Gly1523=
XM_011518248.1:c.4557G>T	XP_011516550.1:p.Gly1519=
XM_011518249.1:c.4464G>T	XP_011516551.1:p.Gly1488=
XM_011518250.1:c.4422G>T	XP_011516552.1:p.Gly1474=
XM_011518251.1:c.3969G>T	XP_011516553.1:p.Gly1323=
XM_011518251.2:c.3969G>T	XP_011516553.1:p.Gly1323=
XM_011518252.1:c.4698G>T	XP_011516554.1:p.Gly1566=
XM_011518252.2:c.4698G>T	XP_011516554.1:p.Gly1566=
XM_011518253.1:c.2631G>T	XP_011516555.1:p.Gly877=
XM_017014287.1:c.4335G>T	XP_016869776.1:p.Gly1445=
XM_017014288.1:c.4188G>T	XP_016869777.1:p.Gly1396=
XR_001746185.1:n.4936G>T
XR_929716.1:n.4936G>T
XR_929717.1:n.4936G>T
XR_929717.2:n.4936G>T