Canonical Allele Identifier: CA1141839189

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209632931_209632934delinsGGGG , CM000663.2:g.209632931_209632934delinsGGGG	GRCh38
NC_000001.10:g.209806276_209806279delinsGGGG , CM000663.1:g.209806276_209806279delinsGGGG	GRCh37
NC_000001.9:g.207872899_207872902delinsGGGG	NCBI36
NG_007116.1:g.24542_24545delinsCCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.628+136_628+139delinsCCCC MANE Select	ENSP00000348384.3:n.628+136_628+139delinsCCCC
ENST00000356082.8:c.628+136_628+139delinsCCCC	ENSP00000348384.3:n.628+136_628+139delinsCCCC
ENST00000367030.7:c.628+136_628+139delinsCCCC	ENSP00000355997.3:n.628+136_628+139delinsCCCC
ENST00000391911.5:c.628+136_628+139delinsCCCC	ENSP00000375778.1:n.628+136_628+139delinsCCCC
NM_000228.2:c.628+136_628+139delinsCCCC	NP_000219.2:n.628+136_628+139delinsCCCC
NM_001017402.1:c.628+136_628+139delinsCCCC	NP_001017402.1:n.628+136_628+139delinsCCCC
NM_001127641.1:c.628+136_628+139delinsCCCC	NP_001121113.1:n.628+136_628+139delinsCCCC
XM_005273124.3:c.628+136_628+139delinsCCCC	XP_005273181.1:n.628+136_628+139delinsCCCC
XM_005273124.4:c.628+136_628+139delinsCCCC	XP_005273181.1:n.628+136_628+139delinsCCCC
XM_017001272.2:c.436+136_436+139delinsCCCC	XP_016856761.1:n.436+136_436+139delinsCCCC
NM_000228.3:c.628+136_628+139delinsCCCC MANE Select	NP_000219.2:n.628+136_628+139delinsCCCC
NM_001017402.2:c.628+136_628+139delinsCCCC	NP_001017402.1:n.628+136_628+139delinsCCCC