Canonical Allele Identifier: CA1510354279

Gene: TLL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.166059991_166059992delinsTG , CM000666.2:g.166059991_166059992delinsTG	GRCh38
NC_000004.11:g.166981143_166981144delinsTG , CM000666.1:g.166981143_166981144delinsTG	GRCh37
NC_000004.10:g.167200593_167200594delinsTG	NCBI36
NG_016278.1:g.191734_191735delinsTG
NG_016278.2:g.191734_191735delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000061240.7:c.1847-37_1847-36delinsTG MANE Select	ENSP00000061240.2:n.1847-37_1847-36delinsTG
ENST00000061240.6:c.1847-37_1847-36delinsTG	ENSP00000061240.2:n.1847-37_1847-36delinsTG
ENST00000507499.5:c.1916-37_1916-36delinsTG	ENSP00000426082.1:n.1916-37_1916-36delinsTG
ENST00000509505.5:c.*1492-37_*1492-36delinsTG	ENSP00000422692.1:n.*1492-37_*1492-36delinsTG
NM_012464.4:c.1847-37_1847-36delinsTG	NP_036596.3:n.1847-37_1847-36delinsTG
XM_011532212.1:c.1847-37_1847-36delinsTG	XP_011530514.1:n.1847-37_1847-36delinsTG
XM_011532213.1:c.1700-37_1700-36delinsTG	XP_011530515.1:n.1700-37_1700-36delinsTG
XM_011532214.1:c.1319-37_1319-36delinsTG	XP_011530516.1:n.1319-37_1319-36delinsTG
XM_017008570.1:c.1700-37_1700-36delinsTG	XP_016864059.1:n.1700-37_1700-36delinsTG
XM_024454194.1:c.1547-37_1547-36delinsTG	XP_024309962.1:n.1547-37_1547-36delinsTG
XM_024454195.1:c.1547-37_1547-36delinsTG	XP_024309963.1:n.1547-37_1547-36delinsTG
NM_012464.5:c.1847-37_1847-36delinsTG MANE Select	NP_036596.3:n.1847-37_1847-36delinsTG