Canonical Allele Identifier: CA2484296305

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618591_209618593delinsCTG , CM000663.2:g.209618591_209618593delinsCTG	GRCh38
NC_000001.10:g.209791936_209791938delinsCTG , CM000663.1:g.209791936_209791938delinsCTG	GRCh37
NC_000001.9:g.207858559_207858561delinsCTG	NCBI36
NG_007116.1:g.38883_38885delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2768_2770delinsCAG MANE Select	ENSP00000348384.3:p.Thr923=
ENST00000356082.8:c.2768_2770delinsCAG	ENSP00000348384.3:p.Thr923=
ENST00000367030.7:c.2768_2770delinsCAG	ENSP00000355997.3:p.Thr923=
ENST00000391911.5:c.2768_2770delinsCAG	ENSP00000375778.1:p.Thr923=
ENST00000455193.1:c.-26_-24delinsCAG	ENSP00000398683.1:n.-26_-24delinsCAG
NM_000228.2:c.2768_2770delinsCAG	NP_000219.2:p.Thr923=
NM_001017402.1:c.2768_2770delinsCAG	NP_001017402.1:p.Thr923=
NM_001127641.1:c.2768_2770delinsCAG	NP_001121113.1:p.Thr923=
XM_005273124.3:c.2768_2770delinsCAG	XP_005273181.1:p.Thr923=
XM_005273124.4:c.2768_2770delinsCAG	XP_005273181.1:p.Thr923=
XM_017001272.2:c.2576_2578delinsCAG	XP_016856761.1:p.Thr859=
NM_000228.3:c.2768_2770delinsCAG MANE Select	NP_000219.2:p.Thr923=
NM_001017402.2:c.2768_2770delinsCAG	NP_001017402.1:p.Thr923=