Canonical Allele Identifier: CA2575887814

Gene: THOC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3027131C>A , CM000678.2:g.3027131C>A	GRCh38
NC_000016.9:g.3077132C>A , CM000678.1:g.3077132C>A	GRCh37
NC_000016.8:g.3017133C>A	NCBI36
NG_052595.1:g.8113C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326266.13:c.700-39C>A MANE Select	ENSP00000326531.8:n.700-39C>A
ENST00000253952.9:c.700-39C>A	ENSP00000253952.9:n.700-39C>A
ENST00000326266.12:c.700-39C>A	ENSP00000326531.8:n.700-39C>A
ENST00000574549.5:c.628-39C>A	ENSP00000458295.1:n.628-39C>A
ENST00000575576.5:c.628-39C>A	ENSP00000460015.1:n.628-39C>A
NM_001142350.1:c.700-39C>A	NP_001135822.1:n.700-39C>A
NM_024339.3:c.700-39C>A	NP_077315.2:n.700-39C>A
NM_001142350.2:c.700-39C>A	NP_001135822.1:n.700-39C>A
NM_001347703.1:c.628-39C>A	NP_001334632.1:n.628-39C>A
NM_001347704.1:c.700-39C>A	NP_001334633.1:n.700-39C>A
NM_024339.4:c.700-39C>A	NP_077315.2:n.700-39C>A
NM_024339.5:c.700-39C>A MANE Select	NP_077315.2:n.700-39C>A
NM_001142350.3:c.700-39C>A	NP_001135822.1:n.700-39C>A
NM_001347703.2:c.628-39C>A	NP_001334632.1:n.628-39C>A
NM_001347704.2:c.700-39C>A	NP_001334633.1:n.700-39C>A