Canonical Allele Identifier: CA1856014720

Gene: TRPM6

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74737424T= , CM000671.2:g.74737424T=	GRCh38
NC_000009.11:g.77352340T= , CM000671.1:g.77352340T=	GRCh37
NC_000009.10:g.76542160T=	NCBI36
NG_017036.1:g.155671A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360774.6:c.5776+983A= MANE Select	ENSP00000354006.1:n.5776+983A=
ENST00000360774.5:c.5776+983A=	ENSP00000354006.1:n.5776+983A=
ENST00000361255.7:c.5761+983A=	ENSP00000354962.3:n.5761+983A=
ENST00000449912.6:c.5761+983A=	ENSP00000396672.2:n.5761+983A=
NM_001177310.1:c.5761+983A=	NP_001170781.1:n.5761+983A=
NM_001177311.1:c.5761+983A=	NP_001170782.1:n.5761+983A=
NM_017662.4:c.5776+983A=	NP_060132.3:n.5776+983A=
XM_011518244.1:c.5773+983A=	XP_011516546.1:n.5773+983A=
XM_011518245.1:c.5683+983A=	XP_011516547.1:n.5683+983A=
XM_011518246.1:c.5653+983A=	XP_011516548.1:n.5653+983A=
XM_011518247.1:c.5647+983A=	XP_011516549.1:n.5647+983A=
XM_011518248.1:c.5635+983A=	XP_011516550.1:n.5635+983A=
XM_011518249.1:c.5542+983A=	XP_011516551.1:n.5542+983A=
XM_011518250.1:c.5500+983A=	XP_011516552.1:n.5500+983A=
XM_011518251.1:c.5047+983A=	XP_011516553.1:n.5047+983A=
XM_011518253.1:c.3709+983A=	XP_011516555.1:n.3709+983A=
XR_929716.1:n.6041A=
XM_011518251.2:c.5047+983A=	XP_011516553.1:n.5047+983A=
XM_017014287.1:c.5413+983A=	XP_016869776.1:n.5413+983A=
XM_017014288.1:c.5266+983A=	XP_016869777.1:n.5266+983A=
XR_001746185.1:n.6041A=
NM_017662.5:c.5776+983A= MANE Select	NP_060132.3:n.5776+983A=
NM_001177310.2:c.5761+983A=	NP_001170781.1:n.5761+983A=
NM_001177311.2:c.5761+983A=	NP_001170782.1:n.5761+983A=