Canonical Allele Identifier: CA790413961

Gene: TLL1

Linked Data

• dbSNP Id: rs1352026247
• MyVariant Identifiers: chr4:g.166830285G>A (hg19) ; chr4:g.165909133G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.165909133G>A , CM000666.2:g.165909133G>A	GRCh38
NC_000004.11:g.166830285G>A , CM000666.1:g.166830285G>A	GRCh37
NC_000004.10:g.167049735G>A	NCBI36
NG_016278.1:g.40876G>A
NG_016278.2:g.40876G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000061240.7:c.169+35060G>A MANE Select	ENSP00000061240.2:n.169+35060G>A
ENST00000061240.6:c.169+35060G>A	ENSP00000061240.2:n.169+35060G>A
ENST00000504560.5:c.170-10701G>A	ENSP00000421732.1:n.170-10701G>A
ENST00000506144.1:c.-132+34081G>A	ENSP00000423748.1:n.-132+34081G>A
ENST00000507499.5:c.169+35060G>A	ENSP00000426082.1:n.169+35060G>A
ENST00000509505.5:c.169+35060G>A	ENSP00000422692.1:n.169+35060G>A
ENST00000513213.5:c.169+35060G>A	ENSP00000422937.1:n.169+35060G>A
NM_001204760.1:c.169+35060G>A	NP_001191689.1:n.169+35060G>A
NM_012464.4:c.169+35060G>A	NP_036596.3:n.169+35060G>A
XM_011532212.1:c.169+35060G>A	XP_011530514.1:n.169+35060G>A
XM_011532213.1:c.-84-10701G>A	XP_011530515.1:n.-84-10701G>A
XM_011532214.1:c.-398+35060G>A	XP_011530516.1:n.-398+35060G>A
XM_017008570.1:c.-84-10701G>A	XP_016864059.1:n.-84-10701G>A
XM_024454194.1:c.-132+35991G>A	XP_024309962.1:n.-132+35991G>A
NM_012464.5:c.169+35060G>A MANE Select	NP_036596.3:n.169+35060G>A
NM_001204760.2:c.169+35060G>A	NP_001191689.1:n.169+35060G>A