Canonical Allele Identifier: CA2484300866

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209629891_209629892delinsGT , CM000663.2:g.209629891_209629892delinsGT	GRCh38
NC_000001.10:g.209803236_209803237delinsGT , CM000663.1:g.209803236_209803237delinsGT	GRCh37
NC_000001.9:g.207869859_207869860delinsGT	NCBI36
NG_007116.1:g.27584_27585delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.977_978delinsAC MANE Select	ENSP00000348384.3:p.His326=
ENST00000356082.8:c.977_978delinsAC	ENSP00000348384.3:p.His326=
ENST00000367030.7:c.977_978delinsAC	ENSP00000355997.3:p.His326=
ENST00000391911.5:c.977_978delinsAC	ENSP00000375778.1:p.His326=
NM_000228.2:c.977_978delinsAC	NP_000219.2:p.His326=
NM_001017402.1:c.977_978delinsAC	NP_001017402.1:p.His326=
NM_001127641.1:c.977_978delinsAC	NP_001121113.1:p.His326=
XM_005273124.3:c.977_978delinsAC	XP_005273181.1:p.His326=
XM_005273124.4:c.977_978delinsAC	XP_005273181.1:p.His326=
XM_017001272.2:c.785_786delinsAC	XP_016856761.1:p.His262=
NM_000228.3:c.977_978delinsAC MANE Select	NP_000219.2:p.His326=
NM_001017402.2:c.977_978delinsAC	NP_001017402.1:p.His326=