Canonical Allele Identifier: CA505415554

Gene: TIMM44

Linked Data

• MyVariant Identifiers: chr19:g.7998814T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7933929T>C , CM000681.2:g.7933929T>C	GRCh38
NC_000019.9:g.7998814T>C , CM000681.1:g.7998814T>C	GRCh37
NC_000019.8:g.7904814T>C	NCBI36
NG_051180.1:g.14895A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.618A>G MANE Select	ENSP00000270538.2:p.Arg206=
ENST00000270538.7:c.618A>G	ENSP00000270538.2:p.Arg206=
ENST00000595831.5:c.605A>G
ENST00000595876.5:c.*306A>G	ENSP00000471596.1:n.*306A>G
ENST00000597926.1:c.522A>G	ENSP00000469389.1:p.Arg174=
ENST00000598675.1:n.24A>G
ENST00000600748.5:n.603A>G
NM_006351.3:c.618A>G	NP_006342.2:p.Arg206=
NM_006351.4:c.618A>G MANE Select	NP_006342.2:p.Arg206=