Canonical Allele Identifier: CA2484298451

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209623965_209623966delinsAG , CM000663.2:g.209623965_209623966delinsAG	GRCh38
NC_000001.10:g.209797310_209797311delinsAG , CM000663.1:g.209797310_209797311delinsAG	GRCh37
NC_000001.9:g.207863933_207863934delinsAG	NCBI36
NG_007116.1:g.33510_33511delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.2011_2012delinsCT MANE Select	ENSP00000348384.3:p.Leu671=
ENST00000356082.8:c.2011_2012delinsCT	ENSP00000348384.3:p.Leu671=
ENST00000367030.7:c.2011_2012delinsCT	ENSP00000355997.3:p.Leu671=
ENST00000391911.5:c.2011_2012delinsCT	ENSP00000375778.1:p.Leu671=
NM_000228.2:c.2011_2012delinsCT	NP_000219.2:p.Leu671=
NM_001017402.1:c.2011_2012delinsCT	NP_001017402.1:p.Leu671=
NM_001127641.1:c.2011_2012delinsCT	NP_001121113.1:p.Leu671=
XM_005273124.3:c.2011_2012delinsCT	XP_005273181.1:p.Leu671=
XM_005273124.4:c.2011_2012delinsCT	XP_005273181.1:p.Leu671=
XM_017001272.2:c.1819_1820delinsCT	XP_016856761.1:p.Leu607=
NM_000228.3:c.2011_2012delinsCT MANE Select	NP_000219.2:p.Leu671=
NM_001017402.2:c.2011_2012delinsCT	NP_001017402.1:p.Leu671=