Canonical Allele Identifier: CA1510347550

Gene: TLL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.166008738T= , CM000666.2:g.166008738T=	GRCh38
NC_000004.11:g.166929890T= , CM000666.1:g.166929890T=	GRCh37
NC_000004.10:g.167149340T=	NCBI36
NG_016278.1:g.140481T=
NG_016278.2:g.140481T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000061240.7:c.917+690T= MANE Select	ENSP00000061240.2:n.917+690T=
ENST00000061240.6:c.917+690T=	ENSP00000061240.2:n.917+690T=
ENST00000507499.5:c.917+690T=	ENSP00000426082.1:n.917+690T=
ENST00000509505.5:c.*562+690T=	ENSP00000422692.1:n.*562+690T=
ENST00000513213.5:c.917+690T=	ENSP00000422937.1:n.917+690T=
NM_001204760.1:c.917+690T=	NP_001191689.1:n.917+690T=
NM_012464.4:c.917+690T=	NP_036596.3:n.917+690T=
XM_011532212.1:c.917+690T=	XP_011530514.1:n.917+690T=
XM_011532213.1:c.770+690T=	XP_011530515.1:n.770+690T=
XM_011532214.1:c.389+690T=	XP_011530516.1:n.389+690T=
XM_017008570.1:c.770+690T=	XP_016864059.1:n.770+690T=
XM_024454194.1:c.617+690T=	XP_024309962.1:n.617+690T=
XM_024454195.1:c.617+690T=	XP_024309963.1:n.617+690T=
NM_012464.5:c.917+690T= MANE Select	NP_036596.3:n.917+690T=
NM_001204760.2:c.917+690T=	NP_001191689.1:n.917+690T=