Canonical Allele Identifier: CA1510302563
Gene: TLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.165909220_165909221delinsAG , CM000666.2:g.165909220_165909221delinsAG GRCh38
NC_000004.11:g.166830372_166830373delinsAG , CM000666.1:g.166830372_166830373delinsAG GRCh37
NC_000004.10:g.167049822_167049823delinsAG NCBI36
NG_016278.1:g.40963_40964delinsAG
NG_016278.2:g.40963_40964delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000061240.7:c.169+35147_169+35148delinsAG MANE Select ENSP00000061240.2:n.169+35147_169+35148de...
ENST00000061240.6:c.169+35147_169+35148delinsAG ENSP00000061240.2:n.169+35147_169+35148de...
ENST00000504560.5:c.170-10614_170-10613delinsAG ENSP00000421732.1:n.170-10614_170-10613de...
ENST00000506144.1:c.-132+34168_-132+34169delinsAG ENSP00000423748.1:n.-132+34168_-132+34169...
ENST00000507499.5:c.169+35147_169+35148delinsAG ENSP00000426082.1:n.169+35147_169+35148de...
ENST00000509505.5:c.169+35147_169+35148delinsAG ENSP00000422692.1:n.169+35147_169+35148de...
ENST00000513213.5:c.169+35147_169+35148delinsAG ENSP00000422937.1:n.169+35147_169+35148de...
NM_001204760.1:c.169+35147_169+35148delinsAG NP_001191689.1:n.169+35147_169+35148delin...
NM_012464.4:c.169+35147_169+35148delinsAG NP_036596.3:n.169+35147_169+35148delinsAG...
XM_011532212.1:c.169+35147_169+35148delinsAG XP_011530514.1:n.169+35147_169+35148delin...
XM_011532213.1:c.-84-10614_-84-10613delinsAG XP_011530515.1:n.-84-10614_-84-10613delin...
XM_011532214.1:c.-398+35147_-398+35148delinsAG XP_011530516.1:n.-398+35147_-398+35148del...
XM_017008570.1:c.-84-10614_-84-10613delinsAG XP_016864059.1:n.-84-10614_-84-10613delin...
XM_024454194.1:c.-132+36078_-132+36079delinsAG XP_024309962.1:n.-132+36078_-132+36079del...
NM_012464.5:c.169+35147_169+35148delinsAG MANE Select NP_036596.3:n.169+35147_169+35148delinsAG...
NM_001204760.2:c.169+35147_169+35148delinsAG NP_001191689.1:n.169+35147_169+35148delin...