Canonical Allele Identifier: CA403700131

Gene: TIMM44

Linked Data

• MyVariant Identifiers: chr19:g.7998881T>C (hg19) ; chr19:g.7933996T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7933996T>C , CM000681.2:g.7933996T>C	GRCh38
NC_000019.9:g.7998881T>C , CM000681.1:g.7998881T>C	GRCh37
NC_000019.8:g.7904881T>C	NCBI36
NG_051180.1:g.14828A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.551A>G MANE Select	ENSP00000270538.2:p.Glu184Gly
ENST00000270538.7:c.551A>G	ENSP00000270538.2:p.Glu184Gly
ENST00000595831.5:c.538A>G
ENST00000595876.5:c.*239A>G	ENSP00000471596.1:n.*239A>G
ENST00000597926.1:c.455A>G	ENSP00000469389.1:p.Glu152Gly
ENST00000600748.5:n.536A>G
NM_006351.3:c.551A>G	NP_006342.2:p.Glu184Gly
NM_006351.4:c.551A>G MANE Select	NP_006342.2:p.Glu184Gly