Canonical Allele Identifier: CA13301216
Gene: TMEM26 HGNC NCBI

Linked Data

dbSNP Id: rs7088627

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61432656T>A , CM000672.2:g.61432656T>A GRCh38
NC_000010.10:g.63192414T>A , CM000672.1:g.63192414T>A GRCh37
NC_000010.9:g.62862420T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000399298.8:c.271-1324A>T MANE Select ENSP00000382237.3:n.271-1324A>T
ENST00000399298.7:c.271-1324A>T ENSP00000382237.3:n.271-1324A>T
ENST00000488505.2:c.271-1324A>T ENSP00000426071.1:n.271-1324A>T
ENST00000503886.5:c.271-1324A>T ENSP00000425286.1:n.271-1324A>T
NM_178505.6:c.271-1324A>T NP_848600.2:n.271-1324A>T
XM_011539450.1:c.271-1324A>T XP_011537752.1:n.271-1324A>T
XM_011539451.1:c.271-1324A>T XP_011537753.1:n.271-1324A>T
XR_246076.1:n.428-1324A>T
XR_945616.1:n.428-1324A>T
NM_178505.7:c.271-1324A>T NP_848600.2:n.271-1324A>T
NR_134507.1:n.640-1324A>T
NR_134508.1:n.640-1324A>T
XM_011539450.2:c.271-1324A>T XP_011537752.1:n.271-1324A>T
XM_017015829.1:c.271-1324A>T XP_016871318.1:n.271-1324A>T
NM_178505.8:c.271-1324A>T MANE Select NP_848600.2:n.271-1324A>T
NR_134507.2:n.571-1324A>T
NR_134508.2:n.571-1324A>T