Canonical Allele Identifier: CA4640651

Gene: TUSC3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.15743623G>C , CM000670.2:g.15743623G>C	GRCh38
NC_000008.10:g.15601132G>C , CM000670.1:g.15601132G>C	GRCh37
NC_000008.9:g.15645503G>C	NCBI36
NG_012141.2:g.208403G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006765.4:c.937+11G>C MANE Select	NP_006756.2:n.937+11G>C
ENST00000503731.6:c.937+11G>C MANE Select	ENSP00000424544.1:n.937+11G>C
NM_001356429.1:c.937+11G>C	NP_001343358.1:n.937+11G>C
NM_001356429.2:c.937+11G>C	NP_001343358.1:n.937+11G>C
NM_006765.3:c.937+11G>C	NP_006756.2:n.937+11G>C
NM_178234.2:c.937+11G>C	NP_839952.1:n.937+11G>C
ENST00000382020.8:c.937+11G>C	ENSP00000371450.4:n.937+11G>C
ENST00000503731.5:c.937+11G>C	ENSP00000424544.1:n.937+11G>C
ENST00000506802.5:c.937+11G>C	ENSP00000425777.1:n.937+11G>C
ENST00000507316.1:n.169+11G>C
ENST00000508446.1:n.241+11G>C
ENST00000510836.5:c.*42+11G>C	ENSP00000426973.1:n.*42+11G>C
ENST00000511342.1:n.83+11G>C
ENST00000511783.2:c.799+11G>C	ENSP00000426880.2:n.799+11G>C
ENST00000515859.5:c.*42+11G>C	ENSP00000420829.1:n.*42+11G>C
XM_011544651.1:c.769+11G>C	XP_011542953.1:n.769+11G>C
XM_011544651.3:c.769+11G>C	XP_011542953.1:n.769+11G>C
XM_011544652.1:c.769+11G>C	XP_011542954.1:n.769+11G>C
XM_011544653.1:c.769+11G>C	XP_011542955.1:n.769+11G>C
XM_011544654.1:c.769+11G>C	XP_011542956.1:n.769+11G>C
XM_017013861.2:c.769+11G>C	XP_016869350.1:n.769+11G>C