Canonical Allele Identifier: CA2321169265

Gene: TIMM44

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7934047G= , CM000681.2:g.7934047G=	GRCh38
NC_000019.9:g.7998932G= , CM000681.1:g.7998932G=	GRCh37
NC_000019.8:g.7904932G=	NCBI36
NG_051180.1:g.14777C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.543+42C= MANE Select	ENSP00000270538.2:n.543+42C=
ENST00000270538.7:c.543+42C=	ENSP00000270538.2:n.543+42C=
ENST00000595831.5:c.530+42C=
ENST00000595876.5:c.*231+42C=	ENSP00000471596.1:n.*231+42C=
ENST00000597926.1:c.447+42C=	ENSP00000469389.1:n.447+42C=
ENST00000600748.5:n.528+42C=
NM_006351.3:c.543+42C=	NP_006342.2:n.543+42C=
NM_006351.4:c.543+42C= MANE Select	NP_006342.2:n.543+42C=