Canonical Allele Identifier: CA109787935

Gene: TLL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.166060491A>G , CM000666.2:g.166060491A>G	GRCh38
NC_000004.11:g.166981643A>G , CM000666.1:g.166981643A>G	GRCh37
NC_000004.10:g.167201093A>G	NCBI36
NG_016278.1:g.192234A>G
NG_016278.2:g.192234A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_012464.5:c.2007+303A>G MANE Select	NP_036596.3:n.2007+303A>G
ENST00000061240.7:c.2007+303A>G MANE Select	ENSP00000061240.2:n.2007+303A>G
NM_012464.4:c.2007+303A>G	NP_036596.3:n.2007+303A>G
ENST00000061240.6:c.2007+303A>G	ENSP00000061240.2:n.2007+303A>G
ENST00000507499.5:c.2076+303A>G	ENSP00000426082.1:n.2076+303A>G
ENST00000509505.5:c.*1652+303A>G	ENSP00000422692.1:n.*1652+303A>G
XM_011532212.1:c.2007+303A>G	XP_011530514.1:n.2007+303A>G
XM_011532213.1:c.1860+303A>G	XP_011530515.1:n.1860+303A>G
XM_011532214.1:c.1479+303A>G	XP_011530516.1:n.1479+303A>G
XM_017008570.1:c.1860+303A>G	XP_016864059.1:n.1860+303A>G
XM_024454194.1:c.1707+303A>G	XP_024309962.1:n.1707+303A>G
XM_024454195.1:c.1707+303A>G	XP_024309963.1:n.1707+303A>G