Canonical Allele Identifier: CA1856028979

Gene: TRPM6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74761731T= , CM000671.2:g.74761731T=	GRCh38
NC_000009.11:g.77376647T= , CM000671.1:g.77376647T=	GRCh37
NC_000009.10:g.76566467T=	NCBI36
NG_017036.1:g.131364A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360774.6:c.4750A= MANE Select	ENSP00000354006.1:p.Lys1584=
ENST00000360774.5:c.4750A=	ENSP00000354006.1:p.Lys1584=
ENST00000361255.7:c.4735A=	ENSP00000354962.3:p.Lys1579=
ENST00000449912.6:c.4735A=	ENSP00000396672.2:p.Lys1579=
NM_001177310.1:c.4735A=	NP_001170781.1:p.Lys1579=
NM_001177311.1:c.4735A=	NP_001170782.1:p.Lys1579=
NM_017662.4:c.4750A=	NP_060132.3:p.Lys1584=
XM_011518244.1:c.4750A=	XP_011516546.1:p.Lys1584=
XM_011518245.1:c.4657A=	XP_011516547.1:p.Lys1553=
XM_011518246.1:c.4750A=	XP_011516548.1:p.Lys1584=
XM_011518247.1:c.4621A=	XP_011516549.1:p.Lys1541=
XM_011518248.1:c.4609A=	XP_011516550.1:p.Lys1537=
XM_011518249.1:c.4516A=	XP_011516551.1:p.Lys1506=
XM_011518250.1:c.4474A=	XP_011516552.1:p.Lys1492=
XM_011518251.1:c.4021A=	XP_011516553.1:p.Lys1341=
XM_011518252.1:c.4750A=	XP_011516554.1:p.Lys1584=
XM_011518253.1:c.2683A=	XP_011516555.1:p.Lys895=
XR_929716.1:n.4988A=
XR_929717.1:n.4988A=
XM_011518251.2:c.4021A=	XP_011516553.1:p.Lys1341=
XM_011518252.2:c.4750A=	XP_011516554.1:p.Lys1584=
XM_017014287.1:c.4387A=	XP_016869776.1:p.Lys1463=
XM_017014288.1:c.4240A=	XP_016869777.1:p.Lys1414=
XR_001746185.1:n.4988A=
XR_929717.2:n.4988A=
NM_017662.5:c.4750A= MANE Select	NP_060132.3:p.Lys1584=
NM_001177310.2:c.4735A=	NP_001170781.1:p.Lys1579=
NM_001177311.2:c.4735A=	NP_001170782.1:p.Lys1579=