Canonical Allele Identifier: CA645516431

Gene: LAMB3

Linked Data

• COSMIC: COSM6440013

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209650080_209650081delinsAA , CM000663.2:g.209650080_209650081delinsAA	GRCh38
NC_000001.10:g.209823425_209823426delinsAA , CM000663.1:g.209823425_209823426delinsAA	GRCh37
NC_000001.9:g.207890048_207890049delinsAA	NCBI36
NG_007116.1:g.7395_7396delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.66_67delinsTT MANE Select	ENSP00000348384.3:p.Arg23Cys
ENST00000356082.8:c.66_67delinsTT	ENSP00000348384.3:p.Arg23Cys
ENST00000367030.7:c.66_67delinsTT	ENSP00000355997.3:p.Arg23Cys
ENST00000391911.5:c.66_67delinsTT	ENSP00000375778.1:p.Arg23Cys
ENST00000415782.1:c.66_67delinsTT	ENSP00000388960.1:p.Arg23Cys
NM_000228.2:c.66_67delinsTT	NP_000219.2:p.Arg23Cys
NM_001017402.1:c.66_67delinsTT	NP_001017402.1:p.Arg23Cys
NM_001127641.1:c.66_67delinsTT	NP_001121113.1:p.Arg23Cys
XM_005273124.3:c.66_67delinsTT	XP_005273181.1:p.Arg23Cys
XM_005273124.4:c.66_67delinsTT	XP_005273181.1:p.Arg23Cys
XM_017001272.2:c.66_67delinsTT	XP_016856761.1:p.Arg23Cys
NM_000228.3:c.66_67delinsTT MANE Select	NP_000219.2:p.Arg23Cys
NM_001017402.2:c.66_67delinsTT	NP_001017402.1:p.Arg23Cys