Canonical Allele Identifier: CA1510354274

Gene: TLL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.166059989C= , CM000666.2:g.166059989C=	GRCh38
NC_000004.11:g.166981141C= , CM000666.1:g.166981141C=	GRCh37
NC_000004.10:g.167200591C=	NCBI36
NG_016278.1:g.191732C=
NG_016278.2:g.191732C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000061240.7:c.1847-39C= MANE Select	ENSP00000061240.2:n.1847-39C=
ENST00000061240.6:c.1847-39C=	ENSP00000061240.2:n.1847-39C=
ENST00000507499.5:c.1916-39C=	ENSP00000426082.1:n.1916-39C=
ENST00000509505.5:c.*1492-39C=	ENSP00000422692.1:n.*1492-39C=
NM_012464.4:c.1847-39C=	NP_036596.3:n.1847-39C=
XM_011532212.1:c.1847-39C=	XP_011530514.1:n.1847-39C=
XM_011532213.1:c.1700-39C=	XP_011530515.1:n.1700-39C=
XM_011532214.1:c.1319-39C=	XP_011530516.1:n.1319-39C=
XM_017008570.1:c.1700-39C=	XP_016864059.1:n.1700-39C=
XM_024454194.1:c.1547-39C=	XP_024309962.1:n.1547-39C=
XM_024454195.1:c.1547-39C=	XP_024309963.1:n.1547-39C=
NM_012464.5:c.1847-39C= MANE Select	NP_036596.3:n.1847-39C=