Canonical Allele Identifier: CA1510354281
Gene: TLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.166059995G= , CM000666.2:g.166059995G= GRCh38
NC_000004.11:g.166981147G= , CM000666.1:g.166981147G= GRCh37
NC_000004.10:g.167200597G= NCBI36
NG_016278.1:g.191738G=
NG_016278.2:g.191738G=

Transcript Alleles

HGVS Amino-acid change
ENST00000061240.7:c.1847-33G= MANE Select ENSP00000061240.2:n.1847-33G=
ENST00000061240.6:c.1847-33G= ENSP00000061240.2:n.1847-33G=
ENST00000507499.5:c.1916-33G= ENSP00000426082.1:n.1916-33G=
ENST00000509505.5:c.*1492-33G= ENSP00000422692.1:n.*1492-33G=
NM_012464.4:c.1847-33G= NP_036596.3:n.1847-33G=
XM_011532212.1:c.1847-33G= XP_011530514.1:n.1847-33G=
XM_011532213.1:c.1700-33G= XP_011530515.1:n.1700-33G=
XM_011532214.1:c.1319-33G= XP_011530516.1:n.1319-33G=
XM_017008570.1:c.1700-33G= XP_016864059.1:n.1700-33G=
XM_024454194.1:c.1547-33G= XP_024309962.1:n.1547-33G=
XM_024454195.1:c.1547-33G= XP_024309963.1:n.1547-33G=
NM_012464.5:c.1847-33G= MANE Select NP_036596.3:n.1847-33G=