Canonical Allele Identifier: CA2484301998

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209632682_209632690delinsCACAGCATA , CM000663.2:g.209632682_209632690delinsCACAGCATA	GRCh38
NC_000001.10:g.209806027_209806035delinsCACAGCATA , CM000663.1:g.209806027_209806035delinsCACAGCATA	GRCh37
NC_000001.9:g.207872650_207872658delinsCACAGCATA	NCBI36
NG_007116.1:g.24786_24794delinsTATGCTGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000356082.9:c.715_723delinsTATGCTGTG MANE Select	ENSP00000348384.3:p.Tyr239=
ENST00000356082.8:c.715_723delinsTATGCTGTG	ENSP00000348384.3:p.Tyr239=
ENST00000367030.7:c.715_723delinsTATGCTGTG	ENSP00000355997.3:p.Tyr239=
ENST00000391911.5:c.715_723delinsTATGCTGTG	ENSP00000375778.1:p.Tyr239=
NM_000228.2:c.715_723delinsTATGCTGTG	NP_000219.2:p.Tyr239=
NM_001017402.1:c.715_723delinsTATGCTGTG	NP_001017402.1:p.Tyr239=
NM_001127641.1:c.715_723delinsTATGCTGTG	NP_001121113.1:p.Tyr239=
XM_005273124.3:c.715_723delinsTATGCTGTG	XP_005273181.1:p.Tyr239=
XM_005273124.4:c.715_723delinsTATGCTGTG	XP_005273181.1:p.Tyr239=
XM_017001272.2:c.523_531delinsTATGCTGTG	XP_016856761.1:p.Tyr175=
NM_000228.3:c.715_723delinsTATGCTGTG MANE Select	NP_000219.2:p.Tyr239=
NM_001017402.2:c.715_723delinsTATGCTGTG	NP_001017402.1:p.Tyr239=