Canonical Allele Identifier: CA14690424

Gene: TOMM40

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44899959C>T , CM000681.2:g.44899959C>T	GRCh38
NC_000019.9:g.45403216C>T , CM000681.1:g.45403216C>T	GRCh37
NC_000019.8:g.50095056C>T	NCBI36
NG_042854.1:g.13740C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426677.7:c.644-771C>T MANE Select	ENSP00000410339.1:n.644-771C>T
ENST00000252487.9:c.644-771C>T	ENSP00000252487.4:n.644-771C>T
ENST00000405636.6:c.644-771C>T	ENSP00000385184.2:n.644-771C>T
ENST00000426677.6:c.644-771C>T	ENSP00000410339.1:n.644-771C>T
ENST00000592041.1:c.160-771C>T
ENST00000592434.5:c.644-771C>T	ENSP00000466084.1:n.644-771C>T
NM_001128916.1:c.644-771C>T	NP_001122388.1:n.644-771C>T
NM_001128917.1:c.644-771C>T	NP_001122389.1:n.644-771C>T
NM_006114.2:c.644-771C>T	NP_006105.1:n.644-771C>T
XM_005258411.2:c.644-771C>T	XP_005258468.1:n.644-771C>T
XM_005258411.4:c.644-771C>T	XP_005258468.1:n.644-771C>T
NM_001128917.2:c.644-771C>T MANE Select	NP_001122389.1:n.644-771C>T
NM_006114.3:c.644-771C>T	NP_006105.1:n.644-771C>T
NM_001128916.2:c.644-771C>T	NP_001122388.1:n.644-771C>T