Canonical Allele Identifier: CA2539844857
Gene: LAMB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209633300_209633301insGTTTCTT , CM000663.2:g.209633300_209633301insGTTTCTT GRCh38
NC_000001.10:g.209806645_209806646insGTTTCTT , CM000663.1:g.209806645_209806646insGTTTCTT GRCh37
NC_000001.9:g.207873268_207873269insGTTTCTT NCBI36
NG_007116.1:g.24175_24176insAAGAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356082.9:c.565-168_565-167insAAGAAAC MANE Select ENSP00000348384.3:n.565-168_565-167insAAGAAAC
ENST00000356082.8:c.565-168_565-167insAAGAAAC ENSP00000348384.3:n.565-168_565-167insAAGAAAC
ENST00000367030.7:c.565-168_565-167insAAGAAAC ENSP00000355997.3:n.565-168_565-167insAAGAAAC
ENST00000391911.5:c.565-168_565-167insAAGAAAC ENSP00000375778.1:n.565-168_565-167insAAGAAAC
NM_000228.2:c.565-168_565-167insAAGAAAC NP_000219.2:n.565-168_565-167insAAGAAAC
NM_001017402.1:c.565-168_565-167insAAGAAAC NP_001017402.1:n.565-168_565-167insAAGAAAC
NM_001127641.1:c.565-168_565-167insAAGAAAC NP_001121113.1:n.565-168_565-167insAAGAAAC
XM_005273124.3:c.565-168_565-167insAAGAAAC XP_005273181.1:n.565-168_565-167insAAGAAAC
XM_005273124.4:c.565-168_565-167insAAGAAAC XP_005273181.1:n.565-168_565-167insAAGAAAC
XM_017001272.2:c.373-168_373-167insAAGAAAC XP_016856761.1:n.373-168_373-167insAAGAAAC
NM_000228.3:c.565-168_565-167insAAGAAAC MANE Select NP_000219.2:n.565-168_565-167insAAGAAAC
NM_001017402.2:c.565-168_565-167insAAGAAAC NP_001017402.1:n.565-168_565-167insAAGAAAC