Canonical Allele Identifier: CA6038508

Gene: TMEM258

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61790539C>T , CM000673.2:g.61790539C>T	GRCh38
NC_000011.9:g.61558011C>T , CM000673.1:g.61558011C>T	GRCh37
NC_000011.8:g.61314587C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014206.4:c.67G>A MANE Select	NP_055021.1:p.Val23Met
ENST00000537328.6:c.67G>A MANE Select	ENSP00000443216.1:p.Val23Met
NM_014206.3:c.67G>A	NP_055021.1:p.Val23Met
ENST00000257262.12:c.67G>A	ENSP00000257262.8:p.Val23Met
ENST00000535042.1:n.65G>A
ENST00000535297.1:c.67G>A	ENSP00000437809.1:p.Val23Met
ENST00000537328.5:c.67G>A	ENSP00000443216.1:p.Val23Met
ENST00000540434.1:n.111G>A
ENST00000541893.5:c.67G>A	ENSP00000441836.1:p.Val23Met
ENST00000543510.1:c.52G>A	ENSP00000443836.1:p.Val18Met
ENST00000545210.5:c.67G>A	ENSP00000445404.1:p.Val23Met