Canonical Allele Identifier: CA2484302028

Gene: LAMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209632761_209632762delinsGT , CM000663.2:g.209632761_209632762delinsGT	GRCh38
NC_000001.10:g.209806106_209806107delinsGT , CM000663.1:g.209806106_209806107delinsGT	GRCh37
NC_000001.9:g.207872729_207872730delinsGT	NCBI36
NG_007116.1:g.24714_24715delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.643_644delinsAC MANE Select	ENSP00000348384.3:p.Thr215=
ENST00000356082.8:c.643_644delinsAC	ENSP00000348384.3:p.Thr215=
ENST00000367030.7:c.643_644delinsAC	ENSP00000355997.3:p.Thr215=
ENST00000391911.5:c.643_644delinsAC	ENSP00000375778.1:p.Thr215=
NM_000228.2:c.643_644delinsAC	NP_000219.2:p.Thr215=
NM_001017402.1:c.643_644delinsAC	NP_001017402.1:p.Thr215=
NM_001127641.1:c.643_644delinsAC	NP_001121113.1:p.Thr215=
XM_005273124.3:c.643_644delinsAC	XP_005273181.1:p.Thr215=
XM_005273124.4:c.643_644delinsAC	XP_005273181.1:p.Thr215=
XM_017001272.2:c.451_452delinsAC	XP_016856761.1:p.Thr151=
NM_000228.3:c.643_644delinsAC MANE Select	NP_000219.2:p.Thr215=
NM_001017402.2:c.643_644delinsAC	NP_001017402.1:p.Thr215=