Canonical Allele Identifier: CA2321169203

Gene: TIMM44

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7933938C= , CM000681.2:g.7933938C=	GRCh38
NC_000019.9:g.7998823C= , CM000681.1:g.7998823C=	GRCh37
NC_000019.8:g.7904823C=	NCBI36
NG_051180.1:g.14886G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.609G= MANE Select	ENSP00000270538.2:p.Arg203=
ENST00000270538.7:c.609G=	ENSP00000270538.2:p.Arg203=
ENST00000595831.5:c.596G=
ENST00000595876.5:c.*297G=	ENSP00000471596.1:n.*297G=
ENST00000597926.1:c.513G=	ENSP00000469389.1:p.Arg171=
ENST00000598675.1:n.15G=
ENST00000600748.5:n.594G=
NM_006351.3:c.609G=	NP_006342.2:p.Arg203=
NM_006351.4:c.609G= MANE Select	NP_006342.2:p.Arg203=