Canonical Allele Identifier: CA2321169235

Gene: TIMM44

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7934002C= , CM000681.2:g.7934002C=	GRCh38
NC_000019.9:g.7998887C= , CM000681.1:g.7998887C=	GRCh37
NC_000019.8:g.7904887C=	NCBI36
NG_051180.1:g.14822G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.545G= MANE Select	ENSP00000270538.2:p.Gly182=
ENST00000270538.7:c.545G=	ENSP00000270538.2:p.Gly182=
ENST00000595831.5:c.532G=
ENST00000595876.5:c.*233G=	ENSP00000471596.1:n.*233G=
ENST00000597926.1:c.449G=	ENSP00000469389.1:p.Gly150=
ENST00000600748.5:n.530G=
NM_006351.3:c.545G=	NP_006342.2:p.Gly182=
NM_006351.4:c.545G= MANE Select	NP_006342.2:p.Gly182=