Canonical Allele Identifier: CA2484295722

Gene: LAMB3

Linked Data

• dbSNP Id: rs1665993901

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209617113_209617118del , CM000663.2:g.209617113_209617118del	GRCh38
NC_000001.10:g.209790458_209790463del , CM000663.1:g.209790458_209790463del	GRCh37
NC_000001.9:g.207857081_207857086del	NCBI36
NG_007116.1:g.40361_40366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356082.9:c.3228+295_3228+300del MANE Select	ENSP00000348384.3:n.3228+295_3228+300del
ENST00000356082.8:c.3228+295_3228+300del	ENSP00000348384.3:n.3228+295_3228+300del
ENST00000367030.7:c.3228+295_3228+300del	ENSP00000355997.3:n.3228+295_3228+300del
ENST00000391911.5:c.3228+295_3228+300del	ENSP00000375778.1:n.3228+295_3228+300del
ENST00000455193.1:c.435+295_435+300del	ENSP00000398683.1:n.435+295_435+300del
NM_000228.2:c.3228+295_3228+300del	NP_000219.2:n.3228+295_3228+300del
NM_001017402.1:c.3228+295_3228+300del	NP_001017402.1:n.3228+295_3228+300del
NM_001127641.1:c.3228+295_3228+300del	NP_001121113.1:n.3228+295_3228+300del
XM_005273124.3:c.3228+295_3228+300del	XP_005273181.1:n.3228+295_3228+300del
XM_005273124.4:c.3228+295_3228+300del	XP_005273181.1:n.3228+295_3228+300del
XM_017001272.2:c.3036+295_3036+300del	XP_016856761.1:n.3036+295_3036+300del
NM_000228.3:c.3228+295_3228+300del MANE Select	NP_000219.2:n.3228+295_3228+300del
NM_001017402.2:c.3228+295_3228+300del	NP_001017402.1:n.3228+295_3228+300del