Canonical Allele Identifier: CA2650322615

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209633275-C-CTTGTCATCTGCTGTGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209633276_209633293dup , CM000663.2:g.209633276_209633293dup	GRCh38
NC_000001.10:g.209806621_209806638dup , CM000663.1:g.209806621_209806638dup	GRCh37
NC_000001.9:g.207873244_207873261dup	NCBI36
NG_007116.1:g.24183_24200dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.565-160_565-143dup MANE Select	ENSP00000348384.3:n.565-160_565-143dup
ENST00000356082.8:c.565-160_565-143dup	ENSP00000348384.3:n.565-160_565-143dup
ENST00000367030.7:c.565-160_565-143dup	ENSP00000355997.3:n.565-160_565-143dup
ENST00000391911.5:c.565-160_565-143dup	ENSP00000375778.1:n.565-160_565-143dup
NM_000228.2:c.565-160_565-143dup	NP_000219.2:n.565-160_565-143dup
NM_001017402.1:c.565-160_565-143dup	NP_001017402.1:n.565-160_565-143dup
NM_001127641.1:c.565-160_565-143dup	NP_001121113.1:n.565-160_565-143dup
XM_005273124.3:c.565-160_565-143dup	XP_005273181.1:n.565-160_565-143dup
XM_005273124.4:c.565-160_565-143dup	XP_005273181.1:n.565-160_565-143dup
XM_017001272.2:c.373-160_373-143dup	XP_016856761.1:n.373-160_373-143dup
NM_000228.3:c.565-160_565-143dup MANE Select	NP_000219.2:n.565-160_565-143dup
NM_001017402.2:c.565-160_565-143dup	NP_001017402.1:n.565-160_565-143dup