Canonical Allele Identifier: CA916393639

Gene: LAMB3

Linked Data

• dbSNP Id: rs1553276931

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626101_209626102del , CM000663.2:g.209626101_209626102del	GRCh38
NC_000001.10:g.209799446_209799447del , CM000663.1:g.209799446_209799447del	GRCh37
NC_000001.9:g.207866069_207866070del	NCBI36
NG_007116.1:g.31376_31377del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1598-74_1598-73del MANE Select	ENSP00000348384.3:n.1598-74_1598-73del
ENST00000356082.8:c.1598-74_1598-73del	ENSP00000348384.3:n.1598-74_1598-73del
ENST00000367030.7:c.1598-74_1598-73del	ENSP00000355997.3:n.1598-74_1598-73del
ENST00000391911.5:c.1598-74_1598-73del	ENSP00000375778.1:n.1598-74_1598-73del
NM_000228.2:c.1598-74_1598-73del	NP_000219.2:n.1598-74_1598-73del
NM_001017402.1:c.1598-74_1598-73del	NP_001017402.1:n.1598-74_1598-73del
NM_001127641.1:c.1598-74_1598-73del	NP_001121113.1:n.1598-74_1598-73del
XM_005273124.3:c.1598-74_1598-73del	XP_005273181.1:n.1598-74_1598-73del
XM_005273124.4:c.1598-74_1598-73del	XP_005273181.1:n.1598-74_1598-73del
XM_017001272.2:c.1406-74_1406-73del	XP_016856761.1:n.1406-74_1406-73del
NM_000228.3:c.1598-74_1598-73del MANE Select	NP_000219.2:n.1598-74_1598-73del
NM_001017402.2:c.1598-74_1598-73del	NP_001017402.1:n.1598-74_1598-73del