Canonical Allele Identifier: CA11667034
Gene: TLL1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12513380

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.165909212G>A , CM000666.2:g.165909212G>A GRCh38
NC_000004.11:g.166830364G>A , CM000666.1:g.166830364G>A GRCh37
NC_000004.10:g.167049814G>A NCBI36
NG_016278.1:g.40955G>A
NG_016278.2:g.40955G>A

Transcript Alleles

HGVS Amino-acid change
NM_001204760.1:c.169+35139G>A VV NP_001191689.1:p.=
NM_012464.4:c.169+35139G>A VV NP_036596.3:p.=
XM_011532212.1:c.169+35139G>A XP_011530514.1:p.=
XM_011532213.1:c.-84-10622G>A XP_011530515.1:p.=
XM_011532214.1:c.-398+35139G>A XP_011530516.1:p.=
XM_017008570.1:c.-84-10622G>A XP_016864059.1:p.=
XM_024454194.1:c.-132+36070G>A XP_024309962.1:p.=
NM_012464.5:c.169+35139G>A VV MANE Preferred NP_036596.3:p.=
ENST00000061240.6:c.169+35139G>A ENSP00000061240.2:p.=
ENST00000504560.5:c.170-10622G>A ENSP00000421732.1:p.=
ENST00000506144.1:c.-132+34160G>A ENSP00000423748.1:p.=
ENST00000507499.5:c.169+35139G>A ENSP00000426082.1:p.=
ENST00000509505.5:c.169+35139G>A ENSP00000422692.1:p.=
ENST00000513213.5:c.169+35139G>A ENSP00000422937.1:p.=