Canonical Allele Identifier: CA2321169219

Gene: TIMM44

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7933967C= , CM000681.2:g.7933967C=	GRCh38
NC_000019.9:g.7998852C= , CM000681.1:g.7998852C=	GRCh37
NC_000019.8:g.7904852C=	NCBI36
NG_051180.1:g.14857G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270538.8:c.580G= MANE Select	ENSP00000270538.2:p.Val194=
ENST00000270538.7:c.580G=	ENSP00000270538.2:p.Val194=
ENST00000595831.5:c.567G=
ENST00000595876.5:c.*268G=	ENSP00000471596.1:n.*268G=
ENST00000597926.1:c.484G=	ENSP00000469389.1:p.Val162=
ENST00000600748.5:n.565G=
NM_006351.3:c.580G=	NP_006342.2:p.Val194=
NM_006351.4:c.580G= MANE Select	NP_006342.2:p.Val194=