Canonical Allele Identifier: CA14597508

Gene: TMX3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.68687521A>G , CM000680.2:g.68687521A>G	GRCh38
NC_000018.9:g.66354758A>G , CM000680.1:g.66354758A>G	GRCh37
NC_000018.8:g.64505738A>G	NCBI36
NG_053149.1:g.32778T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_019022.5:c.736+146T>C MANE Select	NP_061895.3:n.736+146T>C
ENST00000299608.7:c.736+146T>C MANE Select	ENSP00000299608.2:n.736+146T>C
NM_001350514.1:c.655+146T>C	NP_001337443.1:n.655+146T>C
NM_001350514.2:c.655+146T>C	NP_001337443.1:n.655+146T>C
NM_001350515.1:c.313+146T>C	NP_001337444.1:n.313+146T>C
NM_001350515.2:c.313+146T>C	NP_001337444.1:n.313+146T>C
NM_001350516.1:c.313+146T>C	NP_001337445.1:n.313+146T>C
NM_001350516.2:c.313+146T>C	NP_001337445.1:n.313+146T>C
NM_001350517.1:c.313+146T>C	NP_001337446.1:n.313+146T>C
NM_001350517.2:c.313+146T>C	NP_001337446.1:n.313+146T>C
NM_019022.3:c.736+146T>C	NP_061895.3:n.736+146T>C
NM_019022.4:c.736+146T>C	NP_061895.3:n.736+146T>C
ENST00000299608.6:c.736+146T>C	ENSP00000299608.2:n.736+146T>C
ENST00000564631.5:c.*420+146T>C	ENSP00000456587.1:n.*420+146T>C
ENST00000578765.1:n.311+146T>C
XM_005266714.1:c.313+146T>C	XP_005266771.1:n.313+146T>C
XM_011526032.1:c.862+146T>C	XP_011524334.1:n.862+146T>C
XM_011526033.1:c.313+146T>C	XP_011524335.1:n.313+146T>C
XR_935227.1:n.863+146T>C
XR_935227.2:n.867+146T>C