Canonical Allele Identifier: CA2484301189

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209630653_209630654delinsCA , CM000663.2:g.209630653_209630654delinsCA	GRCh38
NC_000001.10:g.209803998_209803999delinsCA , CM000663.1:g.209803998_209803999delinsCA	GRCh37
NC_000001.9:g.207870621_207870622delinsCA	NCBI36
NG_007116.1:g.26822_26823delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.904_905delinsTG MANE Select	ENSP00000348384.3:p.Trp302=
ENST00000356082.8:c.904_905delinsTG	ENSP00000348384.3:p.Trp302=
ENST00000367030.7:c.904_905delinsTG	ENSP00000355997.3:p.Trp302=
ENST00000391911.5:c.904_905delinsTG	ENSP00000375778.1:p.Trp302=
NM_000228.2:c.904_905delinsTG	NP_000219.2:p.Trp302=
NM_001017402.1:c.904_905delinsTG	NP_001017402.1:p.Trp302=
NM_001127641.1:c.904_905delinsTG	NP_001121113.1:p.Trp302=
XM_005273124.3:c.904_905delinsTG	XP_005273181.1:p.Trp302=
XM_005273124.4:c.904_905delinsTG	XP_005273181.1:p.Trp302=
XM_017001272.2:c.712_713delinsTG	XP_016856761.1:p.Trp238=
NM_000228.3:c.904_905delinsTG MANE Select	NP_000219.2:p.Trp302=
NM_001017402.2:c.904_905delinsTG	NP_001017402.1:p.Trp302=