Canonical Allele Identifier: CA1856083785

Gene: TRPM6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74884908T= , CM000671.2:g.74884908T=	GRCh38
NC_000009.11:g.77499824T= , CM000671.1:g.77499824T=	GRCh37
NC_000009.10:g.76689644T=	NCBI36
NG_017036.1:g.8187A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360774.6:c.33+2916A= MANE Select	ENSP00000354006.1:n.33+2916A=
ENST00000359047.2:c.33+2916A=	ENSP00000351942.2:n.33+2916A=
ENST00000360774.5:c.33+2916A=	ENSP00000354006.1:n.33+2916A=
ENST00000361255.7:c.18+2323A=	ENSP00000354962.3:n.18+2323A=
ENST00000449912.6:c.18+2723A=	ENSP00000396672.2:n.18+2723A=
NM_001177310.1:c.18+2723A=	NP_001170781.1:n.18+2723A=
NM_001177311.1:c.18+2323A=	NP_001170782.1:n.18+2323A=
NM_017662.4:c.33+2916A=	NP_060132.3:n.33+2916A=
XM_011518244.1:c.33+2916A=	XP_011516546.1:n.33+2916A=
XM_011518245.1:c.33+2916A=	XP_011516547.1:n.33+2916A=
XM_011518246.1:c.33+2916A=	XP_011516548.1:n.33+2916A=
XM_011518247.1:c.33+2916A=	XP_011516549.1:n.33+2916A=
XM_011518248.1:c.33+2916A=	XP_011516550.1:n.33+2916A=
XM_011518249.1:c.33+2916A=	XP_011516551.1:n.33+2916A=
XM_011518250.1:c.33+2916A=	XP_011516552.1:n.33+2916A=
XM_011518252.1:c.33+2916A=	XP_011516554.1:n.33+2916A=
XM_011518254.1:c.33+2916A=	XP_011516556.1:n.33+2916A=
XM_011518255.1:c.33+2916A=	XP_011516557.1:n.33+2916A=
XR_929716.1:n.271+2916A=
XR_929717.1:n.271+2916A=
XR_929718.1:n.271+2916A=
XM_011518252.2:c.33+2916A=	XP_011516554.1:n.33+2916A=
XM_011518255.2:c.33+2916A=	XP_011516557.1:n.33+2916A=
XM_017014287.1:c.33+2916A=	XP_016869776.1:n.33+2916A=
XM_017014288.1:c.33+2916A=	XP_016869777.1:n.33+2916A=
XM_017014289.1:c.33+2916A=	XP_016869778.1:n.33+2916A=
XR_001746185.1:n.271+2916A=
XR_929717.2:n.271+2916A=
NM_017662.5:c.33+2916A= MANE Select	NP_060132.3:n.33+2916A=
NM_001177310.2:c.18+2723A=	NP_001170781.1:n.18+2723A=
NM_001177311.2:c.18+2323A=	NP_001170782.1:n.18+2323A=