Canonical Allele Identifier: CA2650322253

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209632931-GGGGCAAGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209632939_209632947del , CM000663.2:g.209632939_209632947del	GRCh38
NC_000001.10:g.209806284_209806292del , CM000663.1:g.209806284_209806292del	GRCh37
NC_000001.9:g.207872907_207872915del	NCBI36
NG_007116.1:g.24536_24544del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.628+130_628+138del MANE Select	ENSP00000348384.3:n.628+130_628+138del
ENST00000356082.8:c.628+130_628+138del	ENSP00000348384.3:n.628+130_628+138del
ENST00000367030.7:c.628+130_628+138del	ENSP00000355997.3:n.628+130_628+138del
ENST00000391911.5:c.628+130_628+138del	ENSP00000375778.1:n.628+130_628+138del
NM_000228.2:c.628+130_628+138del	NP_000219.2:n.628+130_628+138del
NM_001017402.1:c.628+130_628+138del	NP_001017402.1:n.628+130_628+138del
NM_001127641.1:c.628+130_628+138del	NP_001121113.1:n.628+130_628+138del
XM_005273124.3:c.628+130_628+138del	XP_005273181.1:n.628+130_628+138del
XM_005273124.4:c.628+130_628+138del	XP_005273181.1:n.628+130_628+138del
XM_017001272.2:c.436+130_436+138del	XP_016856761.1:n.436+130_436+138del
NM_000228.3:c.628+130_628+138del MANE Select	NP_000219.2:n.628+130_628+138del
NM_001017402.2:c.628+130_628+138del	NP_001017402.1:n.628+130_628+138del