Canonical Allele Identifier: CA2578756821
Gene: LAMA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129465146_129465149del , CM000668.2:g.129465146_129465149del GRCh38
NC_000006.11:g.129786291_129786294del , CM000668.1:g.129786291_129786294del GRCh37
NC_000006.10:g.129827984_129827987del NCBI36
NG_008678.1:g.587006_587009del , LRG_409:g.587006_587009del

Transcript Alleles

HGVS Amino-acid Change
ENST00000617695.5:c.7157_7160del
ENST00000618192.5:c.7421_7424del
ENST00000684985.1:n.788_791del
ENST00000688150.1:n.496_499del
ENST00000421865.3:c.7157_7160del
ENST00000421865.2:c.7157_7160del
ENST00000617695.4:c.7157_7160del
ENST00000618192.4:c.7154_7157del
NM_000426.3:c.7157_7160del , LRG_409t1:c.7157_7160del
NM_001079823.1:c.7157_7160del
XM_005266981.2:c.7421_7424del
XM_005266982.2:c.7421_7424del
XM_011535820.1:c.7415_7418del
XM_005266981.3:c.7421_7424del
XM_005266982.3:c.7421_7424del
XM_011535820.2:c.7415_7418del
XM_017010851.2:c.7427_7430del
XM_017010852.1:c.5552_5555del
NM_000426.4:c.7157_7160del
NM_001079823.2:c.7157_7160del