Canonical Allele Identifier: CA2000559347

Gene: TIMM8B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086755C= , CM000673.2:g.112086755C=	GRCh38
NC_000011.9:g.111957479C= , CM000673.1:g.111957479C=	GRCh37
NC_000011.8:g.111462689C=	NCBI36
NG_012337.2:g.4909C=
NG_033145.1:g.5044G=
NG_012337.3:g.4909C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504148.3:c.-32G= MANE Select	ENSP00000422122.2:n.-32G=
ENST00000504148.2:c.-32G=	ENSP00000422122.2:n.-32G=
ENST00000509359.6:c.-32G=	ENSP00000421964.2:n.-32G=
ENST00000541231.1:c.14G=	ENSP00000438455.1:p.Ser5=
NM_012459.2:c.14G=	NP_036591.2:p.Ser5=
NR_028383.1:n.44G=
NM_012459.3:c.-32G=	NP_036591.3:n.-32G=
NR_028383.2:n.2G=
NR_160400.1:n.2G=
NM_012459.4:c.-32G= MANE Select	NP_036591.3:n.-32G=