Canonical Allele Identifier: CA15317392

Gene: TLL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.165994701G>A , CM000666.2:g.165994701G>A	GRCh38
NC_000004.11:g.166915853G>A , CM000666.1:g.166915853G>A	GRCh37
NC_000004.10:g.167135303G>A	NCBI36
NG_016278.1:g.126444G>A
NG_016278.2:g.126444G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012464.5:c.514+168G>A MANE Select	NP_036596.3:n.514+168G>A
ENST00000061240.7:c.514+168G>A MANE Select	ENSP00000061240.2:n.514+168G>A
NM_001204760.1:c.514+168G>A	NP_001191689.1:n.514+168G>A
NM_001204760.2:c.514+168G>A	NP_001191689.1:n.514+168G>A
NM_012464.4:c.514+168G>A	NP_036596.3:n.514+168G>A
ENST00000061240.6:c.514+168G>A	ENSP00000061240.2:n.514+168G>A
ENST00000506144.1:c.214+168G>A	ENSP00000423748.1:n.214+168G>A
ENST00000507499.5:c.514+168G>A	ENSP00000426082.1:n.514+168G>A
ENST00000509505.5:c.*159+168G>A	ENSP00000422692.1:n.*159+168G>A
ENST00000513213.5:c.514+168G>A	ENSP00000422937.1:n.514+168G>A
XM_011532212.1:c.514+168G>A	XP_011530514.1:n.514+168G>A
XM_011532213.1:c.367+168G>A	XP_011530515.1:n.367+168G>A
XM_011532214.1:c.-15+168G>A	XP_011530516.1:n.-15+168G>A
XM_017008570.1:c.367+168G>A	XP_016864059.1:n.367+168G>A
XM_024454194.1:c.214+168G>A	XP_024309962.1:n.214+168G>A
XM_024454195.1:c.214+168G>A	XP_024309963.1:n.214+168G>A