Canonical Allele Identifier: CA373688190

Gene: TRPM6

Linked Data

• MyVariant Identifiers: chr9:g.77416902C>G (hg19) ; chr9:g.74801986C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74801986C>G , CM000671.2:g.74801986C>G	GRCh38
NC_000009.11:g.77416902C>G , CM000671.1:g.77416902C>G	GRCh37
NC_000009.10:g.76606722C>G	NCBI36
NG_017036.1:g.91109G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360774.6:c.1921G>C MANE Select	ENSP00000354006.1:p.Ala641Pro
ENST00000360774.5:c.1921G>C	ENSP00000354006.1:p.Ala641Pro
ENST00000361255.7:c.1906G>C	ENSP00000354962.3:p.Ala636Pro
ENST00000449912.6:c.1906G>C	ENSP00000396672.2:p.Ala636Pro
NM_001177310.1:c.1906G>C	NP_001170781.1:p.Ala636Pro
NM_001177311.1:c.1906G>C	NP_001170782.1:p.Ala636Pro
NM_017662.4:c.1921G>C	NP_060132.3:p.Ala641Pro
XM_011518244.1:c.1921G>C	XP_011516546.1:p.Ala641Pro
XM_011518245.1:c.1828G>C	XP_011516547.1:p.Ala610Pro
XM_011518246.1:c.1921G>C	XP_011516548.1:p.Ala641Pro
XM_011518247.1:c.1921G>C	XP_011516549.1:p.Ala641Pro
XM_011518248.1:c.1780G>C	XP_011516550.1:p.Ala594Pro
XM_011518249.1:c.1687G>C	XP_011516551.1:p.Ala563Pro
XM_011518250.1:c.1921G>C	XP_011516552.1:p.Ala641Pro
XM_011518251.1:c.1192G>C	XP_011516553.1:p.Ala398Pro
XM_011518252.1:c.1921G>C	XP_011516554.1:p.Ala641Pro
XM_011518253.1:c.-143G>C	XP_011516555.1:n.-143G>C
XM_011518254.1:c.1921G>C	XP_011516556.1:p.Ala641Pro
XM_011518255.1:c.1921G>C	XP_011516557.1:p.Ala641Pro
XR_929716.1:n.2159G>C
XR_929717.1:n.2159G>C
XR_929718.1:n.2159G>C
XM_011518251.2:c.1192G>C	XP_011516553.1:p.Ala398Pro
XM_011518252.2:c.1921G>C	XP_011516554.1:p.Ala641Pro
XM_011518255.2:c.1921G>C	XP_011516557.1:p.Ala641Pro
XM_017014287.1:c.1687G>C	XP_016869776.1:p.Ala563Pro
XM_017014288.1:c.1687G>C	XP_016869777.1:p.Ala563Pro
XM_017014289.1:c.1921G>C	XP_016869778.1:p.Ala641Pro
XR_001746185.1:n.2159G>C
XR_929717.2:n.2159G>C
NM_017662.5:c.1921G>C MANE Select	NP_060132.3:p.Ala641Pro
NM_001177310.2:c.1906G>C	NP_001170781.1:p.Ala636Pro
NM_001177311.2:c.1906G>C	NP_001170782.1:p.Ala636Pro