Canonical Allele Identifier: CA5083779
Community Standard Title: NM_017662.5(TRPM6):c.5488-4G>A
Gene: TRPM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.74739453C>T , CM000671.2:g.74739453C>T GRCh38
NC_000009.11:g.77354369C>T , CM000671.1:g.77354369C>T GRCh37
NC_000009.10:g.76544189C>T NCBI36
NG_017036.1:g.153642G>A

Transcript Alleles

HGVS Amino-acid Change
NM_017662.5:c.5488-4G>A MANE Select NP_060132.3:n.5488-4G>A
ENST00000360774.6:c.5488-4G>A MANE Select ENSP00000354006.1:n.5488-4G>A
NM_001177310.1:c.5473-4G>A NP_001170781.1:n.5473-4G>A
NM_001177310.2:c.5473-4G>A NP_001170781.1:n.5473-4G>A
NM_001177311.1:c.5473-4G>A NP_001170782.1:n.5473-4G>A
NM_001177311.2:c.5473-4G>A NP_001170782.1:n.5473-4G>A
NM_017662.4:c.5488-4G>A NP_060132.3:n.5488-4G>A
ENST00000360774.5:c.5488-4G>A ENSP00000354006.1:n.5488-4G>A
ENST00000361255.7:c.5473-4G>A ENSP00000354962.3:n.5473-4G>A
ENST00000449912.6:c.5473-4G>A ENSP00000396672.2:n.5473-4G>A
XM_011518244.1:c.5485-4G>A XP_011516546.1:n.5485-4G>A
XM_011518245.1:c.5395-4G>A XP_011516547.1:n.5395-4G>A
XM_011518246.1:c.5365-4G>A XP_011516548.1:n.5365-4G>A
XM_011518247.1:c.5359-4G>A XP_011516549.1:n.5359-4G>A
XM_011518248.1:c.5347-4G>A XP_011516550.1:n.5347-4G>A
XM_011518249.1:c.5254-4G>A XP_011516551.1:n.5254-4G>A
XM_011518250.1:c.5212-4G>A XP_011516552.1:n.5212-4G>A
XM_011518251.1:c.4759-4G>A XP_011516553.1:n.4759-4G>A
XM_011518251.2:c.4759-4G>A XP_011516553.1:n.4759-4G>A
XM_011518253.1:c.3421-4G>A XP_011516555.1:n.3421-4G>A
XM_017014287.1:c.5125-4G>A XP_016869776.1:n.5125-4G>A
XM_017014288.1:c.4978-4G>A XP_016869777.1:n.4978-4G>A
XR_001746185.1:n.5726-4G>A
XR_929716.1:n.5726-4G>A