Canonical Allele Identifier: CA2321174123

Gene: TIMM44

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7943578C= , CM000681.2:g.7943578C=	GRCh38
NC_000019.9:g.8008463C= , CM000681.1:g.8008463C=	GRCh37
NC_000019.8:g.7914463C=	NCBI36
NG_051180.1:g.5246G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.45+29G= MANE Select	ENSP00000270538.2:n.45+29G=
ENST00000270538.7:c.45+29G=	ENSP00000270538.2:n.45+29G=
ENST00000595831.5:c.29+29G=
ENST00000595876.5:c.45+29G=	ENSP00000471596.1:n.45+29G=
ENST00000597926.1:c.45+29G=	ENSP00000469389.1:n.45+29G=
ENST00000600000.1:n.60+29G=
ENST00000600748.5:n.30+29G=
NM_006351.3:c.45+29G=	NP_006342.2:n.45+29G=
NM_006351.4:c.45+29G= MANE Select	NP_006342.2:n.45+29G=