Canonical Allele Identifier: CA110044321
Gene: TLL1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17047200

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.166008836A>T , CM000666.2:g.166008836A>T GRCh38
NC_000004.10:g.167149438A>T NCBI36
NC_000004.11:g.166929988A>T , CM000666.1:g.166929988A>T GRCh37
NG_016278.1:g.140579A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000061240.6:c.917+788A>T ENSP00000061240.2:p.=
ENST00000507499.5:c.917+788A>T ENSP00000426082.1:p.=
ENST00000509505.5:c.*562+788A>T ENSP00000422692.1:p.=
ENST00000513213.5:c.917+788A>T ENSP00000422937.1:p.=
NM_001204760.1:c.917+788A>T VV NP_001191689.1:p.=
NM_012464.4:c.917+788A>T VV NP_036596.3:p.=
XM_011532212.1:c.917+788A>T XP_011530514.1:p.=
XM_011532213.1:c.770+788A>T XP_011530515.1:p.=
XM_011532214.1:c.389+788A>T XP_011530516.1:p.=