Canonical Allele Identifier: CA2484299325

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626029_209626030delinsAG , CM000663.2:g.209626029_209626030delinsAG	GRCh38
NC_000001.10:g.209799374_209799375delinsAG , CM000663.1:g.209799374_209799375delinsAG	GRCh37
NC_000001.9:g.207865997_207865998delinsAG	NCBI36
NG_007116.1:g.31446_31447delinsCT

Transcript Alleles

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