Canonical Allele Identifier: CA2484299658

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209626853_209626854delinsCT , CM000663.2:g.209626853_209626854delinsCT	GRCh38
NC_000001.10:g.209800198_209800199delinsCT , CM000663.1:g.209800198_209800199delinsCT	GRCh37
NC_000001.9:g.207866821_207866822delinsCT	NCBI36
NG_007116.1:g.30622_30623delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.1597+13_1597+14delinsAG MANE Select	ENSP00000348384.3:n.1597+13_1597+14delinsAG
ENST00000356082.8:c.1597+13_1597+14delinsAG	ENSP00000348384.3:n.1597+13_1597+14delinsAG
ENST00000367030.7:c.1597+13_1597+14delinsAG	ENSP00000355997.3:n.1597+13_1597+14delinsAG
ENST00000391911.5:c.1597+13_1597+14delinsAG	ENSP00000375778.1:n.1597+13_1597+14delinsAG
NM_000228.2:c.1597+13_1597+14delinsAG	NP_000219.2:n.1597+13_1597+14delinsAG
NM_001017402.1:c.1597+13_1597+14delinsAG	NP_001017402.1:n.1597+13_1597+14delinsAG
NM_001127641.1:c.1597+13_1597+14delinsAG	NP_001121113.1:n.1597+13_1597+14delinsAG
XM_005273124.3:c.1597+13_1597+14delinsAG	XP_005273181.1:n.1597+13_1597+14delinsAG
XM_005273124.4:c.1597+13_1597+14delinsAG	XP_005273181.1:n.1597+13_1597+14delinsAG
XM_017001272.2:c.1405+13_1405+14delinsAG	XP_016856761.1:n.1405+13_1405+14delinsAG
NM_000228.3:c.1597+13_1597+14delinsAG MANE Select	NP_000219.2:n.1597+13_1597+14delinsAG
NM_001017402.2:c.1597+13_1597+14delinsAG	NP_001017402.1:n.1597+13_1597+14delinsAG