Canonical Allele Identifier: CA2650320561

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209618338-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618340del , CM000663.2:g.209618340del	GRCh38
NC_000001.10:g.209791685del , CM000663.1:g.209791685del	GRCh37
NC_000001.9:g.207858308del	NCBI36
NG_007116.1:g.39137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2909+113del MANE Select	ENSP00000348384.3:n.2909+113del
ENST00000356082.8:c.2909+113del	ENSP00000348384.3:n.2909+113del
ENST00000367030.7:c.2909+113del	ENSP00000355997.3:n.2909+113del
ENST00000391911.5:c.2909+113del	ENSP00000375778.1:n.2909+113del
ENST00000455193.1:c.116+113del	ENSP00000398683.1:n.116+113del
NM_000228.2:c.2909+113del	NP_000219.2:n.2909+113del
NM_001017402.1:c.2909+113del	NP_001017402.1:n.2909+113del
NM_001127641.1:c.2909+113del	NP_001121113.1:n.2909+113del
XM_005273124.3:c.2909+113del	XP_005273181.1:n.2909+113del
XM_005273124.4:c.2909+113del	XP_005273181.1:n.2909+113del
XM_017001272.2:c.2717+113del	XP_016856761.1:n.2717+113del
NM_000228.3:c.2909+113del MANE Select	NP_000219.2:n.2909+113del
NM_001017402.2:c.2909+113del	NP_001017402.1:n.2909+113del