Canonical Allele Identifier: CA2680313966
Gene: LAMA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129315621dup , CM000668.2:g.129315621dup GRCh38
NC_000006.11:g.129636766dup , CM000668.1:g.129636766dup GRCh37
NC_000006.10:g.129678459dup NCBI36
NG_008678.1:g.437481dup , LRG_409:g.437481dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000617695.5:c.3701dup ENSP00000481744.2:p.Tyr1234Ter
ENST00000618192.5:c.3965dup ENSP00000480802.2:p.Tyr1322Ter
ENST00000421865.3:c.3701dup MANE Select ENSP00000400365.2:p.Tyr1234Ter
ENST00000421865.2:c.3701dup ENSP00000400365.2:p.Tyr1234Ter
ENST00000617695.4:c.3701dup ENSP00000481744.1:p.Tyr1234Ter
ENST00000618192.4:c.3701dup ENSP00000480802.1:p.Tyr1234Ter
NM_000426.3:c.3701dup , LRG_409t1:c.3701dup NP_000417.2:p.Tyr1234Ter
NM_001079823.1:c.3701dup NP_001073291.1:p.Tyr1234Ter
XM_005266981.2:c.3965dup XP_005267038.1:p.Tyr1322Ter
XM_005266982.2:c.3965dup XP_005267039.1:p.Tyr1322Ter
XM_011535820.1:c.3965dup XP_011534122.1:p.Tyr1322Ter
XM_005266981.3:c.3965dup XP_005267038.1:p.Tyr1322Ter
XM_005266982.3:c.3965dup XP_005267039.1:p.Tyr1322Ter
XM_011535820.2:c.3965dup XP_011534122.1:p.Tyr1322Ter
XM_017010851.2:c.3971dup XP_016866340.1:p.Tyr1324Ter
XM_017010852.1:c.2096dup XP_016866341.1:p.Tyr699Ter
XM_017010853.1:c.3965dup XP_016866342.1:p.Tyr1322Ter
NM_000426.4:c.3701dup MANE Select NP_000417.3:p.Tyr1234Ter
NM_001079823.2:c.3701dup NP_001073291.2:p.Tyr1234Ter