Canonical Allele Identifier: CA2573998137

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209650212-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209650214del , CM000663.2:g.209650214del	GRCh38
NC_000001.10:g.209823559del , CM000663.1:g.209823559del	GRCh37
NC_000001.9:g.207890182del	NCBI36
NG_007116.1:g.7263del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.29-95del MANE Select	ENSP00000348384.3:n.29-95del
ENST00000356082.8:c.29-95del	ENSP00000348384.3:n.29-95del
ENST00000367030.7:c.29-95del	ENSP00000355997.3:n.29-95del
ENST00000391911.5:c.29-95del	ENSP00000375778.1:n.29-95del
ENST00000415782.1:c.29-95del	ENSP00000388960.1:n.29-95del
NM_000228.2:c.29-95del	NP_000219.2:n.29-95del
NM_001017402.1:c.29-95del	NP_001017402.1:n.29-95del
NM_001127641.1:c.29-95del	NP_001121113.1:n.29-95del
XM_005273124.3:c.29-95del	XP_005273181.1:n.29-95del
XM_005273124.4:c.29-95del	XP_005273181.1:n.29-95del
XM_017001272.2:c.29-95del	XP_016856761.1:n.29-95del
NM_000228.3:c.29-95del MANE Select	NP_000219.2:n.29-95del
NM_001017402.2:c.29-95del	NP_001017402.1:n.29-95del