Canonical Allele Identifier: CA1510302523

Gene: TLL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.165909195_165909196delinsAG , CM000666.2:g.165909195_165909196delinsAG	GRCh38
NC_000004.11:g.166830347_166830348delinsAG , CM000666.1:g.166830347_166830348delinsAG	GRCh37
NC_000004.10:g.167049797_167049798delinsAG	NCBI36
NG_016278.1:g.40938_40939delinsAG
NG_016278.2:g.40938_40939delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000061240.7:c.169+35122_169+35123delinsAG MANE Select	ENSP00000061240.2:n.169+35122_169+35123delinsAG
ENST00000061240.6:c.169+35122_169+35123delinsAG	ENSP00000061240.2:n.169+35122_169+35123delinsAG
ENST00000504560.5:c.170-10639_170-10638delinsAG	ENSP00000421732.1:n.170-10639_170-10638delinsAG
ENST00000506144.1:c.-132+34143_-132+34144delinsAG	ENSP00000423748.1:n.-132+34143_-132+34144delinsAG
ENST00000507499.5:c.169+35122_169+35123delinsAG	ENSP00000426082.1:n.169+35122_169+35123delinsAG
ENST00000509505.5:c.169+35122_169+35123delinsAG	ENSP00000422692.1:n.169+35122_169+35123delinsAG
ENST00000513213.5:c.169+35122_169+35123delinsAG	ENSP00000422937.1:n.169+35122_169+35123delinsAG
NM_001204760.1:c.169+35122_169+35123delinsAG	NP_001191689.1:n.169+35122_169+35123delinsAG
NM_012464.4:c.169+35122_169+35123delinsAG	NP_036596.3:n.169+35122_169+35123delinsAG
XM_011532212.1:c.169+35122_169+35123delinsAG	XP_011530514.1:n.169+35122_169+35123delinsAG
XM_011532213.1:c.-84-10639_-84-10638delinsAG	XP_011530515.1:n.-84-10639_-84-10638delinsAG
XM_011532214.1:c.-398+35122_-398+35123delinsAG	XP_011530516.1:n.-398+35122_-398+35123delinsAG
XM_017008570.1:c.-84-10639_-84-10638delinsAG	XP_016864059.1:n.-84-10639_-84-10638delinsAG
XM_024454194.1:c.-132+36053_-132+36054delinsAG	XP_024309962.1:n.-132+36053_-132+36054delinsAG
NM_012464.5:c.169+35122_169+35123delinsAG MANE Select	NP_036596.3:n.169+35122_169+35123delinsAG
NM_001204760.2:c.169+35122_169+35123delinsAG	NP_001191689.1:n.169+35122_169+35123delinsAG