Canonical Allele Identifier: CA2484300851

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209629856_209629857delinsGC , CM000663.2:g.209629856_209629857delinsGC	GRCh38
NC_000001.10:g.209803201_209803202delinsGC , CM000663.1:g.209803201_209803202delinsGC	GRCh37
NC_000001.9:g.207869824_207869825delinsGC	NCBI36
NG_007116.1:g.27619_27620delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1012_1013delinsGC MANE Select	ENSP00000348384.3:p.Ala338=
ENST00000356082.8:c.1012_1013delinsGC	ENSP00000348384.3:p.Ala338=
ENST00000367030.7:c.1012_1013delinsGC	ENSP00000355997.3:p.Ala338=
ENST00000391911.5:c.1012_1013delinsGC	ENSP00000375778.1:p.Ala338=
NM_000228.2:c.1012_1013delinsGC	NP_000219.2:p.Ala338=
NM_001017402.1:c.1012_1013delinsGC	NP_001017402.1:p.Ala338=
NM_001127641.1:c.1012_1013delinsGC	NP_001121113.1:p.Ala338=
XM_005273124.3:c.1012_1013delinsGC	XP_005273181.1:p.Ala338=
XM_005273124.4:c.1012_1013delinsGC	XP_005273181.1:p.Ala338=
XM_017001272.2:c.820_821delinsGC	XP_016856761.1:p.Ala274=
NM_000228.3:c.1012_1013delinsGC MANE Select	NP_000219.2:p.Ala338=
NM_001017402.2:c.1012_1013delinsGC	NP_001017402.1:p.Ala338=