Canonical Allele Identifier: CA2000559266

Gene: TIMM8B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086727T= , CM000673.2:g.112086727T=	GRCh38
NC_000011.9:g.111957451T= , CM000673.1:g.111957451T=	GRCh37
NC_000011.8:g.111462661T=	NCBI36
NG_012337.2:g.4881T=
NG_033145.1:g.5072A=
NG_012337.3:g.4881T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504148.3:c.-4A= MANE Select	ENSP00000422122.2:n.-4A=
ENST00000504148.2:c.-4A=	ENSP00000422122.2:n.-4A=
ENST00000509359.6:c.-4A=	ENSP00000421964.2:n.-4A=
ENST00000541231.1:c.42A=	ENSP00000438455.1:p.Arg14=
NM_012459.2:c.42A=	NP_036591.2:p.Arg14=
NR_028383.1:n.72A=
NM_012459.3:c.-4A=	NP_036591.3:n.-4A=
NR_028383.2:n.30A=
NR_160400.1:n.30A=
NM_012459.4:c.-4A= MANE Select	NP_036591.3:n.-4A=