Canonical Allele Identifier: CA2650322222

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209632896-A-ACCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209632899_209632902dup , CM000663.2:g.209632899_209632902dup	GRCh38
NC_000001.10:g.209806244_209806247dup , CM000663.1:g.209806244_209806247dup	GRCh37
NC_000001.9:g.207872867_207872870dup	NCBI36
NG_007116.1:g.24576_24579dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.629-124_629-121dup MANE Select	ENSP00000348384.3:n.629-124_629-121dup
ENST00000356082.8:c.629-124_629-121dup	ENSP00000348384.3:n.629-124_629-121dup
ENST00000367030.7:c.629-124_629-121dup	ENSP00000355997.3:n.629-124_629-121dup
ENST00000391911.5:c.629-124_629-121dup	ENSP00000375778.1:n.629-124_629-121dup
NM_000228.2:c.629-124_629-121dup	NP_000219.2:n.629-124_629-121dup
NM_001017402.1:c.629-124_629-121dup	NP_001017402.1:n.629-124_629-121dup
NM_001127641.1:c.629-124_629-121dup	NP_001121113.1:n.629-124_629-121dup
XM_005273124.3:c.629-124_629-121dup	XP_005273181.1:n.629-124_629-121dup
XM_005273124.4:c.629-124_629-121dup	XP_005273181.1:n.629-124_629-121dup
XM_017001272.2:c.437-124_437-121dup	XP_016856761.1:n.437-124_437-121dup
NM_000228.3:c.629-124_629-121dup MANE Select	NP_000219.2:n.629-124_629-121dup
NM_001017402.2:c.629-124_629-121dup	NP_001017402.1:n.629-124_629-121dup