Canonical Allele Identifier: CA2575887815

Gene: THOC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3027144C>G , CM000678.2:g.3027144C>G	GRCh38
NC_000016.9:g.3077145C>G , CM000678.1:g.3077145C>G	GRCh37
NC_000016.8:g.3017146C>G	NCBI36
NG_052595.1:g.8126C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326266.13:c.700-26C>G MANE Select	ENSP00000326531.8:n.700-26C>G
ENST00000253952.9:c.700-26C>G	ENSP00000253952.9:n.700-26C>G
ENST00000326266.12:c.700-26C>G	ENSP00000326531.8:n.700-26C>G
ENST00000574549.5:c.628-26C>G	ENSP00000458295.1:n.628-26C>G
ENST00000575576.5:c.628-26C>G	ENSP00000460015.1:n.628-26C>G
NM_001142350.1:c.700-26C>G	NP_001135822.1:n.700-26C>G
NM_024339.3:c.700-26C>G	NP_077315.2:n.700-26C>G
NM_001142350.2:c.700-26C>G	NP_001135822.1:n.700-26C>G
NM_001347703.1:c.628-26C>G	NP_001334632.1:n.628-26C>G
NM_001347704.1:c.700-26C>G	NP_001334633.1:n.700-26C>G
NM_024339.4:c.700-26C>G	NP_077315.2:n.700-26C>G
NM_024339.5:c.700-26C>G MANE Select	NP_077315.2:n.700-26C>G
NM_001142350.3:c.700-26C>G	NP_001135822.1:n.700-26C>G
NM_001347703.2:c.628-26C>G	NP_001334632.1:n.628-26C>G
NM_001347704.2:c.700-26C>G	NP_001334633.1:n.700-26C>G