Canonical Allele Identifier: CA2650320628

Gene: LAMB3

Linked Data

• gnomAD v4: 1-209618635-A-ATAGTGGCTGCATCAGTGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209618636_209618654dup , CM000663.2:g.209618636_209618654dup	GRCh38
NC_000001.10:g.209791981_209791999dup , CM000663.1:g.209791981_209791999dup	GRCh37
NC_000001.9:g.207858604_207858622dup	NCBI36
NG_007116.1:g.38822_38840dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.2707_2725dup MANE Select	ENSP00000348384.3:p.Ile909ArgfsTer3
ENST00000356082.8:c.2707_2725dup	ENSP00000348384.3:p.Ile909ArgfsTer3
ENST00000367030.7:c.2707_2725dup	ENSP00000355997.3:p.Ile909ArgfsTer3
ENST00000391911.5:c.2707_2725dup	ENSP00000375778.1:p.Ile909ArgfsTer3
ENST00000455193.1:c.-87_-69dup	ENSP00000398683.1:n.-87_-69dup
NM_000228.2:c.2707_2725dup	NP_000219.2:p.Ile909ArgfsTer3
NM_001017402.1:c.2707_2725dup	NP_001017402.1:p.Ile909ArgfsTer3
NM_001127641.1:c.2707_2725dup	NP_001121113.1:p.Ile909ArgfsTer3
XM_005273124.3:c.2707_2725dup	XP_005273181.1:p.Ile909ArgfsTer3
XM_005273124.4:c.2707_2725dup	XP_005273181.1:p.Ile909ArgfsTer3
XM_017001272.2:c.2515_2533dup	XP_016856761.1:p.Ile845ArgfsTer3
NM_000228.3:c.2707_2725dup MANE Select	NP_000219.2:p.Ile909ArgfsTer3
NM_001017402.2:c.2707_2725dup	NP_001017402.1:p.Ile909ArgfsTer3