Canonical Allele Identifier: CA1856063453

Gene: TRPM6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74840148G= , CM000671.2:g.74840148G=	GRCh38
NC_000009.11:g.77455064G= , CM000671.1:g.77455064G=	GRCh37
NC_000009.10:g.76644884G=	NCBI36
NG_017036.1:g.52947C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360774.6:c.420C= MANE Select	ENSP00000354006.1:p.Ile140=
ENST00000359047.2:c.420C=	ENSP00000351942.2:p.Ile140=
ENST00000360774.5:c.420C=	ENSP00000354006.1:p.Ile140=
ENST00000361255.7:c.405C=	ENSP00000354962.3:p.Ile135=
ENST00000449912.6:c.405C=	ENSP00000396672.2:p.Ile135=
NM_001177310.1:c.405C=	NP_001170781.1:p.Ile135=
NM_001177311.1:c.405C=	NP_001170782.1:p.Ile135=
NM_017662.4:c.420C=	NP_060132.3:p.Ile140=
XM_011518244.1:c.420C=	XP_011516546.1:p.Ile140=
XM_011518245.1:c.420C=	XP_011516547.1:p.Ile140=
XM_011518246.1:c.420C=	XP_011516548.1:p.Ile140=
XM_011518247.1:c.420C=	XP_011516549.1:p.Ile140=
XM_011518248.1:c.420C=	XP_011516550.1:p.Ile140=
XM_011518249.1:c.420C=	XP_011516551.1:p.Ile140=
XM_011518250.1:c.420C=	XP_011516552.1:p.Ile140=
XM_011518252.1:c.420C=	XP_011516554.1:p.Ile140=
XM_011518254.1:c.420C=	XP_011516556.1:p.Ile140=
XM_011518255.1:c.420C=	XP_011516557.1:p.Ile140=
XR_929716.1:n.658C=
XR_929717.1:n.658C=
XR_929718.1:n.658C=
XM_011518252.2:c.420C=	XP_011516554.1:p.Ile140=
XM_011518255.2:c.420C=	XP_011516557.1:p.Ile140=
XM_017014287.1:c.420C=	XP_016869776.1:p.Ile140=
XM_017014288.1:c.420C=	XP_016869777.1:p.Ile140=
XM_017014289.1:c.420C=	XP_016869778.1:p.Ile140=
XR_001746185.1:n.658C=
XR_929717.2:n.658C=
NM_017662.5:c.420C= MANE Select	NP_060132.3:p.Ile140=
NM_001177310.2:c.405C=	NP_001170781.1:p.Ile135=
NM_001177311.2:c.405C=	NP_001170782.1:p.Ile135=