Canonical Allele Identifier: CA2650322950

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209634549-GGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209634551_209634552del , CM000663.2:g.209634551_209634552del	GRCh38
NC_000001.10:g.209807896_209807897del , CM000663.1:g.209807896_209807897del	GRCh37
NC_000001.9:g.207874519_207874520del	NCBI36
NG_007116.1:g.22925_22926del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.460_461del MANE Select	ENSP00000348384.3:p.Thr154LeufsTer27
ENST00000356082.8:c.460_461del	ENSP00000348384.3:p.Thr154LeufsTer27
ENST00000367030.7:c.460_461del	ENSP00000355997.3:p.Thr154LeufsTer27
ENST00000391911.5:c.460_461del	ENSP00000375778.1:p.Thr154LeufsTer27
ENST00000415782.1:c.460_461del	ENSP00000388960.1:p.Thr154LeufsTer27
NM_000228.2:c.460_461del	NP_000219.2:p.Thr154LeufsTer27
NM_001017402.1:c.460_461del	NP_001017402.1:p.Thr154LeufsTer27
NM_001127641.1:c.460_461del	NP_001121113.1:p.Thr154LeufsTer27
XM_005273124.3:c.460_461del	XP_005273181.1:p.Thr154LeufsTer27
XM_005273124.4:c.460_461del	XP_005273181.1:p.Thr154LeufsTer27
XM_017001272.2:c.373-1418_373-1417del	XP_016856761.1:n.373-1418_373-1417del
NM_000228.3:c.460_461del MANE Select	NP_000219.2:p.Thr154LeufsTer27
NM_001017402.2:c.460_461del	NP_001017402.1:p.Thr154LeufsTer27