Canonical Allele Identifier: CA2650320361
Gene: LAMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209617767_209617777dup , CM000663.2:g.209617767_209617777dup GRCh38
NC_000001.10:g.209791112_209791122dup , CM000663.1:g.209791112_209791122dup GRCh37
NC_000001.9:g.207857735_207857745dup NCBI36
NG_007116.1:g.39704_39714dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.3051+135_3051+145dup MANE Select ENSP00000348384.3:n.3051+135_3051+145dup
ENST00000356082.8:c.3051+135_3051+145dup ENSP00000348384.3:n.3051+135_3051+145dup
ENST00000367030.7:c.3051+135_3051+145dup ENSP00000355997.3:n.3051+135_3051+145dup
ENST00000391911.5:c.3051+135_3051+145dup ENSP00000375778.1:n.3051+135_3051+145dup
ENST00000455193.1:c.258+135_258+145dup ENSP00000398683.1:n.258+135_258+145dup
NM_000228.2:c.3051+135_3051+145dup NP_000219.2:n.3051+135_3051+145dup
NM_001017402.1:c.3051+135_3051+145dup NP_001017402.1:n.3051+135_3051+145dup
NM_001127641.1:c.3051+135_3051+145dup NP_001121113.1:n.3051+135_3051+145dup
XM_005273124.3:c.3051+135_3051+145dup XP_005273181.1:n.3051+135_3051+145dup
XM_005273124.4:c.3051+135_3051+145dup XP_005273181.1:n.3051+135_3051+145dup
XM_017001272.2:c.2859+135_2859+145dup XP_016856761.1:n.2859+135_2859+145dup
NM_000228.3:c.3051+135_3051+145dup MANE Select NP_000219.2:n.3051+135_3051+145dup
NM_001017402.2:c.3051+135_3051+145dup NP_001017402.1:n.3051+135_3051+145dup