Canonical Allele Identifier: CA2650319016

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209615002-TGCCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209615010_209615014del , CM000663.2:g.209615010_209615014del	GRCh38
NC_000001.10:g.209788355_209788359del , CM000663.1:g.209788355_209788359del	GRCh37
NC_000001.9:g.207854978_207854982del	NCBI36
NG_007116.1:g.42469_42473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.*264_*268del MANE Select	ENSP00000348384.3:n.*264_*268del
ENST00000356082.8:c.*264_*268del	ENSP00000348384.3:n.*264_*268del
ENST00000367030.7:c.*264_*268del	ENSP00000355997.3:n.*264_*268del
ENST00000391911.5:c.*264_*268del	ENSP00000375778.1:n.*264_*268del
NM_000228.2:c.*264_*268del	NP_000219.2:n.*264_*268del
NM_001017402.1:c.*264_*268del	NP_001017402.1:n.*264_*268del
NM_001127641.1:c.*264_*268del	NP_001121113.1:n.*264_*268del
XM_005273124.3:c.*264_*268del	XP_005273181.1:n.*264_*268del
XM_005273124.4:c.*264_*268del	XP_005273181.1:n.*264_*268del
XM_017001272.2:c.*264_*268del	XP_016856761.1:n.*264_*268del
NM_000228.3:c.*264_*268del MANE Select	NP_000219.2:n.*264_*268del
NM_001017402.2:c.*264_*268del	NP_001017402.1:n.*264_*268del