Canonical Allele Identifier: CA2650320792

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209618862-CCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618863_209618865del , CM000663.2:g.209618863_209618865del	GRCh38
NC_000001.10:g.209792208_209792210del , CM000663.1:g.209792208_209792210del	GRCh37
NC_000001.9:g.207858831_207858833del	NCBI36
NG_007116.1:g.38611_38613del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2702-206_2702-204del MANE Select	ENSP00000348384.3:n.2702-206_2702-204del
ENST00000356082.8:c.2702-206_2702-204del	ENSP00000348384.3:n.2702-206_2702-204del
ENST00000367030.7:c.2702-206_2702-204del	ENSP00000355997.3:n.2702-206_2702-204del
ENST00000391911.5:c.2702-206_2702-204del	ENSP00000375778.1:n.2702-206_2702-204del
NM_000228.2:c.2702-206_2702-204del	NP_000219.2:n.2702-206_2702-204del
NM_001017402.1:c.2702-206_2702-204del	NP_001017402.1:n.2702-206_2702-204del
NM_001127641.1:c.2702-206_2702-204del	NP_001121113.1:n.2702-206_2702-204del
XM_005273124.3:c.2702-206_2702-204del	XP_005273181.1:n.2702-206_2702-204del
XM_005273124.4:c.2702-206_2702-204del	XP_005273181.1:n.2702-206_2702-204del
XM_017001272.2:c.2510-206_2510-204del	XP_016856761.1:n.2510-206_2510-204del
NM_000228.3:c.2702-206_2702-204del MANE Select	NP_000219.2:n.2702-206_2702-204del
NM_001017402.2:c.2702-206_2702-204del	NP_001017402.1:n.2702-206_2702-204del