Canonical Allele Identifier: CA2000559253

Gene: TIMM8B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086721C= , CM000673.2:g.112086721C=	GRCh38
NC_000011.9:g.111957445C= , CM000673.1:g.111957445C=	GRCh37
NC_000011.8:g.111462655C=	NCBI36
NG_012337.2:g.4875C=
NG_033145.1:g.5078G=
NG_012337.3:g.4875C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504148.3:c.3G= MANE Select	ENSP00000422122.2:p.Met1=
ENST00000504148.2:c.3G=	ENSP00000422122.2:p.Met1=
ENST00000507614.1:n.2G=
ENST00000509359.6:c.3G=	ENSP00000421964.2:p.Met1=
ENST00000541231.1:c.48G=	ENSP00000438455.1:p.Met16=
NM_012459.2:c.48G=	NP_036591.2:p.Met16=
NR_028383.1:n.78G=
NM_012459.3:c.3G=	NP_036591.3:p.Met1=
NR_028383.2:n.36G=
NR_160400.1:n.36G=
NM_012459.4:c.3G= MANE Select	NP_036591.3:p.Met1=