Canonical Allele Identifier: CA556060103

Gene: TLL1

Linked Data

• dbSNP Id: rs1404543960
• gnomAD v2: 4-166830350-AAAAAG-A
• gnomAD v3: 4-165909198-AAAAAG-A
• gnomAD v4: 4-165909198-AAAAAG-A
• MyVariant Identifiers: chr4:g.166830351_166830355del (hg19) ; chr4:g.165909199_165909203del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.165909206_165909210del , CM000666.2:g.165909206_165909210del	GRCh38
NC_000004.11:g.166830358_166830362del , CM000666.1:g.166830358_166830362del	GRCh37
NC_000004.10:g.167049808_167049812del	NCBI36
NG_016278.1:g.40949_40953del
NG_016278.2:g.40949_40953del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000061240.7:c.169+35133_169+35137del MANE Select	ENSP00000061240.2:n.169+35133_169+35137del
ENST00000061240.6:c.169+35133_169+35137del	ENSP00000061240.2:n.169+35133_169+35137del
ENST00000504560.5:c.170-10628_170-10624del	ENSP00000421732.1:n.170-10628_170-10624del
ENST00000506144.1:c.-132+34154_-132+34158del	ENSP00000423748.1:n.-132+34154_-132+34158del
ENST00000507499.5:c.169+35133_169+35137del	ENSP00000426082.1:n.169+35133_169+35137del
ENST00000509505.5:c.169+35133_169+35137del	ENSP00000422692.1:n.169+35133_169+35137del
ENST00000513213.5:c.169+35133_169+35137del	ENSP00000422937.1:n.169+35133_169+35137del
NM_001204760.1:c.169+35133_169+35137del	NP_001191689.1:n.169+35133_169+35137del
NM_012464.4:c.169+35133_169+35137del	NP_036596.3:n.169+35133_169+35137del
XM_011532212.1:c.169+35133_169+35137del	XP_011530514.1:n.169+35133_169+35137del
XM_011532213.1:c.-84-10628_-84-10624del	XP_011530515.1:n.-84-10628_-84-10624del
XM_011532214.1:c.-398+35133_-398+35137del	XP_011530516.1:n.-398+35133_-398+35137del
XM_017008570.1:c.-84-10628_-84-10624del	XP_016864059.1:n.-84-10628_-84-10624del
XM_024454194.1:c.-132+36064_-132+36068del	XP_024309962.1:n.-132+36064_-132+36068del
NM_012464.5:c.169+35133_169+35137del MANE Select	NP_036596.3:n.169+35133_169+35137del
NM_001204760.2:c.169+35133_169+35137del	NP_001191689.1:n.169+35133_169+35137del