Canonical Allele Identifier: CA12377540

Gene: L3MBTL3

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.130027974C>T , CM000668.2:g.130027974C>T	GRCh38
NC_000006.11:g.130349119C>T , CM000668.1:g.130349119C>T	GRCh37
NC_000006.10:g.130390812C>T	NCBI36
NG_051942.1:g.14606C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361794.7:c.-16+5669C>T MANE Select	ENSP00000354526.2:n.-16+5669C>T
ENST00000368136.3:c.-16+5669C>T	ENSP00000357118.2:n.-16+5669C>T
ENST00000674039.1:c.-16+5669C>T	ENSP00000501028.1:n.-16+5669C>T
ENST00000361794.6:c.-16+5669C>T	ENSP00000354526.2:n.-16+5669C>T
ENST00000368136.2:c.-16+5669C>T	ENSP00000357118.2:n.-16+5669C>T
ENST00000368139.6:c.-16+7306C>T	ENSP00000357121.2:n.-16+7306C>T
ENST00000526019.5:c.-16+5669C>T	ENSP00000436706.1:n.-16+5669C>T
ENST00000526087.5:c.-16+5669C>T	ENSP00000436617.1:n.-16+5669C>T
ENST00000528385.5:c.-16+5669C>T	ENSP00000433257.1:n.-16+5669C>T
ENST00000529410.5:c.-16+5669C>T	ENSP00000431962.1:n.-16+5669C>T
ENST00000533560.5:c.-16+5669C>T	ENSP00000437185.1:n.-16+5669C>T
NM_001007102.2:c.-16+5669C>T	NP_001007103.1:n.-16+5669C>T
NM_032438.2:c.-16+5669C>T	NP_115814.1:n.-16+5669C>T
XM_005267161.3:c.-16+5669C>T	XP_005267218.1:n.-16+5669C>T
XM_006715576.2:c.-16+5669C>T	XP_006715639.1:n.-16+5669C>T
XM_006715578.2:c.-16+5669C>T	XP_006715641.1:n.-16+5669C>T
XM_011536179.1:c.-16+5669C>T	XP_011534481.1:n.-16+5669C>T
XM_011536180.1:c.-16+5669C>T	XP_011534482.1:n.-16+5669C>T
XM_011536181.1:c.-16+5669C>T	XP_011534483.1:n.-16+5669C>T
XM_011536182.1:c.-16+5669C>T	XP_011534484.1:n.-16+5669C>T
XM_011536183.1:c.-16+5669C>T	XP_011534485.1:n.-16+5669C>T
XM_011536184.1:c.-16+5669C>T	XP_011534486.1:n.-16+5669C>T
NM_001007102.3:c.-16+5669C>T	NP_001007103.1:n.-16+5669C>T
NM_001346550.1:c.-16+5669C>T	NP_001333479.1:n.-16+5669C>T
NM_001346551.1:c.-16+5669C>T	NP_001333480.1:n.-16+5669C>T
NM_032438.3:c.-16+5669C>T	NP_115814.1:n.-16+5669C>T
XM_005267161.4:c.-16+5669C>T	XP_005267218.1:n.-16+5669C>T
XM_006715576.3:c.-16+5669C>T	XP_006715639.1:n.-16+5669C>T
XM_006715578.3:c.-16+5669C>T	XP_006715641.1:n.-16+5669C>T
XM_011536179.3:c.-16+5669C>T	XP_011534481.1:n.-16+5669C>T
XM_011536180.2:c.-16+5669C>T	XP_011534482.1:n.-16+5669C>T
XM_011536181.2:c.-16+5669C>T	XP_011534483.1:n.-16+5669C>T
XM_011536183.2:c.-16+5669C>T	XP_011534485.1:n.-16+5669C>T
XM_011536184.2:c.-16+5669C>T	XP_011534486.1:n.-16+5669C>T
NM_001007102.4:c.-16+5669C>T	NP_001007103.1:n.-16+5669C>T
NM_032438.4:c.-16+5669C>T MANE Select	NP_115814.1:n.-16+5669C>T
NM_001346550.2:c.-16+5669C>T	NP_001333479.1:n.-16+5669C>T
NM_001346551.2:c.-16+5669C>T	NP_001333480.1:n.-16+5669C>T