Canonical Allele Identifier: CA1510302464
Gene: TLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.165909151C= , CM000666.2:g.165909151C= GRCh38
NC_000004.11:g.166830303C= , CM000666.1:g.166830303C= GRCh37
NC_000004.10:g.167049753C= NCBI36
NG_016278.1:g.40894C=
NG_016278.2:g.40894C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000061240.7:c.169+35078C= MANE Select ENSP00000061240.2:n.169+35078C=
ENST00000061240.6:c.169+35078C= ENSP00000061240.2:n.169+35078C=
ENST00000504560.5:c.170-10683C= ENSP00000421732.1:n.170-10683C=
ENST00000506144.1:c.-132+34099C= ENSP00000423748.1:n.-132+34099C=
ENST00000507499.5:c.169+35078C= ENSP00000426082.1:n.169+35078C=
ENST00000509505.5:c.169+35078C= ENSP00000422692.1:n.169+35078C=
ENST00000513213.5:c.169+35078C= ENSP00000422937.1:n.169+35078C=
NM_001204760.1:c.169+35078C= NP_001191689.1:n.169+35078C=
NM_012464.4:c.169+35078C= NP_036596.3:n.169+35078C=
XM_011532212.1:c.169+35078C= XP_011530514.1:n.169+35078C=
XM_011532213.1:c.-84-10683C= XP_011530515.1:n.-84-10683C=
XM_011532214.1:c.-398+35078C= XP_011530516.1:n.-398+35078C=
XM_017008570.1:c.-84-10683C= XP_016864059.1:n.-84-10683C=
XM_024454194.1:c.-132+36009C= XP_024309962.1:n.-132+36009C=
NM_012464.5:c.169+35078C= MANE Select NP_036596.3:n.169+35078C=
NM_001204760.2:c.169+35078C= NP_001191689.1:n.169+35078C=