Canonical Allele Identifier: CA505415613

Gene: TIMM44

Linked Data

• MyVariant Identifiers: chr19:g.7998865T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7933980T>C , CM000681.2:g.7933980T>C	GRCh38
NC_000019.9:g.7998865T>C , CM000681.1:g.7998865T>C	GRCh37
NC_000019.8:g.7904865T>C	NCBI36
NG_051180.1:g.14844A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.567A>G MANE Select	ENSP00000270538.2:p.Glu189=
ENST00000270538.7:c.567A>G	ENSP00000270538.2:p.Glu189=
ENST00000595831.5:c.554A>G
ENST00000595876.5:c.*255A>G	ENSP00000471596.1:n.*255A>G
ENST00000597926.1:c.471A>G	ENSP00000469389.1:p.Glu157=
ENST00000600748.5:n.552A>G
NM_006351.3:c.567A>G	NP_006342.2:p.Glu189=
NM_006351.4:c.567A>G MANE Select	NP_006342.2:p.Glu189=