Canonical Allele Identifier: CA2321169216

Gene: TIMM44

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7933959T= , CM000681.2:g.7933959T=	GRCh38
NC_000019.9:g.7998844T= , CM000681.1:g.7998844T=	GRCh37
NC_000019.8:g.7904844T=	NCBI36
NG_051180.1:g.14865A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.588A= MANE Select	ENSP00000270538.2:p.Gly196=
ENST00000270538.7:c.588A=	ENSP00000270538.2:p.Gly196=
ENST00000595831.5:c.575A=
ENST00000595876.5:c.*276A=	ENSP00000471596.1:n.*276A=
ENST00000597926.1:c.492A=	ENSP00000469389.1:p.Gly164=
ENST00000600748.5:n.573A=
NM_006351.3:c.588A=	NP_006342.2:p.Gly196=
NM_006351.4:c.588A= MANE Select	NP_006342.2:p.Gly196=