Canonical Allele Identifier: CA1070540426
Gene: TLL1 HGNC NCBI

Linked Data

dbSNP Id: rs1732407256

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.165909130dup , CM000666.2:g.165909130dup GRCh38
NC_000004.11:g.166830282dup , CM000666.1:g.166830282dup GRCh37
NC_000004.10:g.167049732dup NCBI36
NG_016278.1:g.40873dup
NG_016278.2:g.40873dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000061240.7:c.169+35057dup MANE Select ENSP00000061240.2:n.169+35057dup
ENST00000061240.6:c.169+35057dup ENSP00000061240.2:n.169+35057dup
ENST00000504560.5:c.170-10704dup ENSP00000421732.1:n.170-10704dup
ENST00000506144.1:c.-132+34078dup ENSP00000423748.1:n.-132+34078dup
ENST00000507499.5:c.169+35057dup ENSP00000426082.1:n.169+35057dup
ENST00000509505.5:c.169+35057dup ENSP00000422692.1:n.169+35057dup
ENST00000513213.5:c.169+35057dup ENSP00000422937.1:n.169+35057dup
NM_001204760.1:c.169+35057dup NP_001191689.1:n.169+35057dup
NM_012464.4:c.169+35057dup NP_036596.3:n.169+35057dup
XM_011532212.1:c.169+35057dup XP_011530514.1:n.169+35057dup
XM_011532213.1:c.-84-10704dup XP_011530515.1:n.-84-10704dup
XM_011532214.1:c.-398+35057dup XP_011530516.1:n.-398+35057dup
XM_017008570.1:c.-84-10704dup XP_016864059.1:n.-84-10704dup
XM_024454194.1:c.-132+35988dup XP_024309962.1:n.-132+35988dup
NM_012464.5:c.169+35057dup MANE Select NP_036596.3:n.169+35057dup
NM_001204760.2:c.169+35057dup NP_001191689.1:n.169+35057dup