Canonical Allele Identifier: CA373670643

Gene: TRPM6

Linked Data

• MyVariant Identifiers: chr9:g.77397327G>C (hg19) ; chr9:g.74782411G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.74782411G>C , CM000671.2:g.74782411G>C	GRCh38
NC_000009.11:g.77397327G>C , CM000671.1:g.77397327G>C	GRCh37
NC_000009.10:g.76587147G>C	NCBI36
NG_017036.1:g.110684C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360774.6:c.3160C>G MANE Select	ENSP00000354006.1:p.Leu1054Val
ENST00000360774.5:c.3160C>G	ENSP00000354006.1:p.Leu1054Val
ENST00000361255.7:c.3145C>G	ENSP00000354962.3:p.Leu1049Val
ENST00000449912.6:c.3145C>G	ENSP00000396672.2:p.Leu1049Val
NM_001177310.1:c.3145C>G	NP_001170781.1:p.Leu1049Val
NM_001177311.1:c.3145C>G	NP_001170782.1:p.Leu1049Val
NM_017662.4:c.3160C>G	NP_060132.3:p.Leu1054Val
XM_011518244.1:c.3160C>G	XP_011516546.1:p.Leu1054Val
XM_011518245.1:c.3067C>G	XP_011516547.1:p.Leu1023Val
XM_011518246.1:c.3160C>G	XP_011516548.1:p.Leu1054Val
XM_011518247.1:c.3031C>G	XP_011516549.1:p.Leu1011Val
XM_011518248.1:c.3019C>G	XP_011516550.1:p.Leu1007Val
XM_011518249.1:c.2926C>G	XP_011516551.1:p.Leu976Val
XM_011518250.1:c.2884C>G	XP_011516552.1:p.Leu962Val
XM_011518251.1:c.2431C>G	XP_011516553.1:p.Leu811Val
XM_011518252.1:c.3160C>G	XP_011516554.1:p.Leu1054Val
XM_011518253.1:c.1093C>G	XP_011516555.1:p.Leu365Val
XM_011518254.1:c.3160C>G	XP_011516556.1:p.Leu1054Val
XM_011518255.1:c.3160C>G	XP_011516557.1:p.Leu1054Val
XR_929716.1:n.3398C>G
XR_929717.1:n.3398C>G
XR_929718.1:n.3332+268C>G
XM_011518251.2:c.2431C>G	XP_011516553.1:p.Leu811Val
XM_011518252.2:c.3160C>G	XP_011516554.1:p.Leu1054Val
XM_011518255.2:c.3160C>G	XP_011516557.1:p.Leu1054Val
XM_017014287.1:c.2797C>G	XP_016869776.1:p.Leu933Val
XM_017014288.1:c.2650C>G	XP_016869777.1:p.Leu884Val
XM_017014289.1:c.3160C>G	XP_016869778.1:p.Leu1054Val
XR_001746185.1:n.3398C>G
XR_929717.2:n.3398C>G
NM_017662.5:c.3160C>G MANE Select	NP_060132.3:p.Leu1054Val
NM_001177310.2:c.3145C>G	NP_001170781.1:p.Leu1049Val
NM_001177311.2:c.3145C>G	NP_001170782.1:p.Leu1049Val