Canonical Allele Identifier: CA11667062

Gene: TLL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.166075262G>A , CM000666.2:g.166075262G>A	GRCh38
NC_000004.11:g.166996414G>A , CM000666.1:g.166996414G>A	GRCh37
NC_000004.10:g.167215864G>A	NCBI36
NG_016278.1:g.207005G>A
NG_016278.2:g.207005G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012464.5:c.2314+259G>A MANE Select	NP_036596.3:n.2314+259G>A
ENST00000061240.7:c.2314+259G>A MANE Select	ENSP00000061240.2:n.2314+259G>A
NM_012464.4:c.2314+259G>A	NP_036596.3:n.2314+259G>A
ENST00000061240.6:c.2314+259G>A	ENSP00000061240.2:n.2314+259G>A
ENST00000507499.5:c.2383+259G>A	ENSP00000426082.1:n.2383+259G>A
ENST00000509505.5:c.*1959+259G>A	ENSP00000422692.1:n.*1959+259G>A
XM_011532212.1:c.2398+259G>A	XP_011530514.1:n.2398+259G>A
XM_011532213.1:c.2251+259G>A	XP_011530515.1:n.2251+259G>A
XM_011532214.1:c.1786+259G>A	XP_011530516.1:n.1786+259G>A
XM_017008570.1:c.2167+259G>A	XP_016864059.1:n.2167+259G>A
XM_024454194.1:c.2014+259G>A	XP_024309962.1:n.2014+259G>A
XM_024454195.1:c.2014+259G>A	XP_024309963.1:n.2014+259G>A