Canonical Allele Identifier: CA2484301218

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209630728_209630729delinsTC , CM000663.2:g.209630728_209630729delinsTC	GRCh38
NC_000001.10:g.209804073_209804074delinsTC , CM000663.1:g.209804073_209804074delinsTC	GRCh37
NC_000001.9:g.207870696_207870697delinsTC	NCBI36
NG_007116.1:g.26747_26748delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.829_830delinsGA MANE Select	ENSP00000348384.3:p.Asp277=
ENST00000356082.8:c.829_830delinsGA	ENSP00000348384.3:p.Asp277=
ENST00000367030.7:c.829_830delinsGA	ENSP00000355997.3:p.Asp277=
ENST00000391911.5:c.829_830delinsGA	ENSP00000375778.1:p.Asp277=
NM_000228.2:c.829_830delinsGA	NP_000219.2:p.Asp277=
NM_001017402.1:c.829_830delinsGA	NP_001017402.1:p.Asp277=
NM_001127641.1:c.829_830delinsGA	NP_001121113.1:p.Asp277=
XM_005273124.3:c.829_830delinsGA	XP_005273181.1:p.Asp277=
XM_005273124.4:c.829_830delinsGA	XP_005273181.1:p.Asp277=
XM_017001272.2:c.637_638delinsGA	XP_016856761.1:p.Asp213=
NM_000228.3:c.829_830delinsGA MANE Select	NP_000219.2:p.Asp277=
NM_001017402.2:c.829_830delinsGA	NP_001017402.1:p.Asp277=