Canonical Allele Identifier: CA2484309335

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209649991_209649992delinsAG , CM000663.2:g.209649991_209649992delinsAG	GRCh38
NC_000001.10:g.209823336_209823337delinsAG , CM000663.1:g.209823336_209823337delinsAG	GRCh37
NC_000001.9:g.207889959_207889960delinsAG	NCBI36
NG_007116.1:g.7484_7485delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.155_156delinsCT MANE Select	ENSP00000348384.3:p.Pro52=
ENST00000356082.8:c.155_156delinsCT	ENSP00000348384.3:p.Pro52=
ENST00000367030.7:c.155_156delinsCT	ENSP00000355997.3:p.Pro52=
ENST00000391911.5:c.155_156delinsCT	ENSP00000375778.1:p.Pro52=
ENST00000415782.1:c.155_156delinsCT	ENSP00000388960.1:p.Pro52=
NM_000228.2:c.155_156delinsCT	NP_000219.2:p.Pro52=
NM_001017402.1:c.155_156delinsCT	NP_001017402.1:p.Pro52=
NM_001127641.1:c.155_156delinsCT	NP_001121113.1:p.Pro52=
XM_005273124.3:c.155_156delinsCT	XP_005273181.1:p.Pro52=
XM_005273124.4:c.155_156delinsCT	XP_005273181.1:p.Pro52=
XM_017001272.2:c.155_156delinsCT	XP_016856761.1:p.Pro52=
NM_000228.3:c.155_156delinsCT MANE Select	NP_000219.2:p.Pro52=
NM_001017402.2:c.155_156delinsCT	NP_001017402.1:p.Pro52=