Canonical Allele Identifier: CA505415680

Gene: TIMM44

Linked Data

• MyVariant Identifiers: chr19:g.7998911del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7934026del , CM000681.2:g.7934026del	GRCh38
NC_000019.9:g.7998911del , CM000681.1:g.7998911del	GRCh37
NC_000019.8:g.7904911del	NCBI36
NG_051180.1:g.14798del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.544-23del MANE Select	ENSP00000270538.2:n.544-23del
ENST00000270538.7:c.544-23del	ENSP00000270538.2:n.544-23del
ENST00000595831.5:c.531-23del
ENST00000595876.5:c.*232-23del	ENSP00000471596.1:n.*232-23del
ENST00000597926.1:c.448-23del	ENSP00000469389.1:n.448-23del
ENST00000600748.5:n.529-23del
NM_006351.3:c.544-23del	NP_006342.2:n.544-23del
NM_006351.4:c.544-23del MANE Select	NP_006342.2:n.544-23del