Canonical Allele Identifier: CA2321169193

Gene: TIMM44

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7933915G= , CM000681.2:g.7933915G=	GRCh38
NC_000019.9:g.7998800G= , CM000681.1:g.7998800G=	GRCh37
NC_000019.8:g.7904800G=	NCBI36
NG_051180.1:g.14909C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.632C= MANE Select	ENSP00000270538.2:p.Thr211=
ENST00000270538.7:c.632C=	ENSP00000270538.2:p.Thr211=
ENST00000595831.5:c.619C=
ENST00000595876.5:c.*320C=	ENSP00000471596.1:n.*320C=
ENST00000597926.1:c.536C=	ENSP00000469389.1:p.Thr179=
ENST00000598675.1:n.38C=
ENST00000600748.5:n.617C=
NM_006351.3:c.632C=	NP_006342.2:p.Thr211=
NM_006351.4:c.632C= MANE Select	NP_006342.2:p.Thr211=