Canonical Allele Identifier: CA505244708

Gene: TIMM44

Linked Data

• MyVariant Identifiers: chr19:g.8008513A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7943628A>G , CM000681.2:g.7943628A>G	GRCh38
NC_000019.9:g.8008513A>G , CM000681.1:g.8008513A>G	GRCh37
NC_000019.8:g.7914513A>G	NCBI36
NG_051180.1:g.5196T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.24T>C MANE Select	ENSP00000270538.2:p.Ser8=
ENST00000270538.7:c.24T>C	ENSP00000270538.2:p.Ser8=
ENST00000595831.5:c.8T>C
ENST00000595876.5:c.24T>C	ENSP00000471596.1:p.Ser8=
ENST00000597926.1:c.24T>C	ENSP00000469389.1:p.Ser8=
ENST00000600000.1:n.39T>C
ENST00000600748.5:n.9T>C
NM_006351.3:c.24T>C	NP_006342.2:p.Ser8=
NM_006351.4:c.24T>C MANE Select	NP_006342.2:p.Ser8=