Canonical Allele Identifier: CA730844272

Gene: LAMB3

Linked Data

• dbSNP Id: rs1281014528
• MyVariant Identifiers: chr1:g.209788551_209788554del (hg19) ; chr1:g.209615206_209615209del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209615207_209615210del , CM000663.2:g.209615207_209615210del	GRCh38
NC_000001.10:g.209788552_209788555del , CM000663.1:g.209788552_209788555del	GRCh37
NC_000001.9:g.207855175_207855178del	NCBI36
NG_007116.1:g.42267_42270del

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.*62_*65del MANE Select	ENSP00000348384.3:n.*62_*65del
ENST00000356082.8:c.*62_*65del	ENSP00000348384.3:n.*62_*65del
ENST00000367030.7:c.*62_*65del	ENSP00000355997.3:n.*62_*65del
ENST00000391911.5:c.*62_*65del	ENSP00000375778.1:n.*62_*65del
NM_000228.2:c.*62_*65del	NP_000219.2:n.*62_*65del
NM_001017402.1:c.*62_*65del	NP_001017402.1:n.*62_*65del
NM_001127641.1:c.*62_*65del	NP_001121113.1:n.*62_*65del
XM_005273124.3:c.*62_*65del	XP_005273181.1:n.*62_*65del
XM_005273124.4:c.*62_*65del	XP_005273181.1:n.*62_*65del
XM_017001272.2:c.*62_*65del	XP_016856761.1:n.*62_*65del
NM_000228.3:c.*62_*65del MANE Select	NP_000219.2:n.*62_*65del
NM_001017402.2:c.*62_*65del	NP_001017402.1:n.*62_*65del