Canonical Allele Identifier: CA1977489105

Gene: TMEM258

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61790331T= , CM000673.2:g.61790331T=	GRCh38
NC_000011.9:g.61557803T= , CM000673.1:g.61557803T=	GRCh37
NC_000011.8:g.61314379T=	NCBI36
NG_047038.1:g.42695T=

Transcript Alleles

HGVS	Amino-acid Change
NM_014206.4:c.113+162A= MANE Select	NP_055021.1:n.113+162A=
ENST00000537328.6:c.113+162A= MANE Select	ENSP00000443216.1:n.113+162A=
NM_014206.3:c.113+162A=	NP_055021.1:n.113+162A=
ENST00000257262.12:c.113+162A=	ENSP00000257262.8:n.113+162A=
ENST00000535042.1:n.111+162A=
ENST00000535297.1:c.*81+44A=	ENSP00000437809.1:n.*81+44A=
ENST00000537328.5:c.113+162A=	ENSP00000443216.1:n.113+162A=
ENST00000540434.1:n.319A=
ENST00000541893.5:c.*33+92A=	ENSP00000441836.1:n.*33+92A=
ENST00000543510.1:c.98+162A=	ENSP00000443836.1:n.98+162A=
ENST00000545210.5:c.*81+44A=	ENSP00000445404.1:n.*81+44A=