Canonical Allele Identifier: CA2747561631

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209614997dup , CM000663.2:g.209614997dup	GRCh38
NC_000001.10:g.209788342dup , CM000663.1:g.209788342dup	GRCh37
NC_000001.9:g.207854965dup	NCBI36
NG_007116.1:g.42483dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.*278dup MANE Select	ENSP00000348384.3:n.*278dup
ENST00000356082.8:c.*278dup	ENSP00000348384.3:n.*278dup
ENST00000367030.7:c.*278dup	ENSP00000355997.3:n.*278dup
ENST00000391911.5:c.*278dup	ENSP00000375778.1:n.*278dup
NM_000228.2:c.*278dup	NP_000219.2:n.*278dup
NM_001017402.1:c.*278dup	NP_001017402.1:n.*278dup
NM_001127641.1:c.*278dup	NP_001121113.1:n.*278dup
XM_005273124.3:c.*278dup	XP_005273181.1:n.*278dup
XM_005273124.4:c.*278dup	XP_005273181.1:n.*278dup
XM_017001272.2:c.*278dup	XP_016856761.1:n.*278dup
NM_000228.3:c.*278dup MANE Select	NP_000219.2:n.*278dup
NM_001017402.2:c.*278dup	NP_001017402.1:n.*278dup