Canonical Allele Identifier: CA1663193606
Gene: LAMA2 HGNC NCBI

Linked Data

dbSNP Id: rs1786759720

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129513394_129513395dup , CM000668.2:g.129513394_129513395dup GRCh38
NC_000006.11:g.129834539_129834540dup , CM000668.1:g.129834539_129834540dup GRCh37
NC_000006.10:g.129876232_129876233dup NCBI36
NG_008678.1:g.635254_635255dup , LRG_409:g.635254_635255dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000494137.2:c.1053+901_1053+902dup ENSP00000510626.1:n.1053+901_1053+902dup
ENST00000498257.6:c.1053+901_1053+902dup ENSP00000510533.1:n.1053+901_1053+902dup
ENST00000617695.5:c.8976+901_8976+902dup ENSP00000481744.2:n.8976+901_8976+902dup
ENST00000618192.5:c.9252+901_9252+902dup ENSP00000480802.2:n.9252+901_9252+902dup
ENST00000688198.1:n.1966+901_1966+902dup
ENST00000688799.1:c.1053+901_1053+902dup ENSP00000508458.1:n.1053+901_1053+902dup
ENST00000690858.1:n.2883_2884dup
ENST00000693461.1:n.1325+901_1325+902dup
ENST00000421865.3:c.8988+901_8988+902dup MANE Select ENSP00000400365.2:n.8988+901_8988+902dup
ENST00000421865.2:c.8988+901_8988+902dup ENSP00000400365.2:n.8988+901_8988+902dup
ENST00000617695.4:c.8976+901_8976+902dup ENSP00000481744.1:n.8976+901_8976+902dup
ENST00000618192.4:c.8985+901_8985+902dup ENSP00000480802.1:n.8985+901_8985+902dup
NM_000426.3:c.8988+901_8988+902dup , LRG_409t1:c.8988+901_8988+902dup NP_000417.2:n.8988+901_8988+902dup
NM_001079823.1:c.8976+901_8976+902dup NP_001073291.1:n.8976+901_8976+902dup
XM_005266981.2:c.9252+901_9252+902dup XP_005267038.1:n.9252+901_9252+902dup
XM_005266982.2:c.9240+901_9240+902dup XP_005267039.1:n.9240+901_9240+902dup
XM_011535820.1:c.9246+901_9246+902dup XP_011534122.1:n.9246+901_9246+902dup
XR_942984.1:n.1460+9082_1460+9083dup
XR_942985.1:n.1324+9082_1324+9083dup
XM_005266981.3:c.9252+901_9252+902dup XP_005267038.1:n.9252+901_9252+902dup
XM_005266982.3:c.9240+901_9240+902dup XP_005267039.1:n.9240+901_9240+902dup
XM_011535820.2:c.9246+901_9246+902dup XP_011534122.1:n.9246+901_9246+902dup
XM_017010851.2:c.9258+901_9258+902dup XP_016866340.1:n.9258+901_9258+902dup
XM_017010852.1:c.7383+901_7383+902dup XP_016866341.1:n.7383+901_7383+902dup
XR_001743859.1:n.3900+9082_3900+9083dup
XR_001743860.1:n.1179+9082_1179+9083dup
XR_001743861.1:n.1346+9082_1346+9083dup
XR_001743863.1:n.883-10604_883-10603dup
XR_002956395.1:n.9131+9082_9131+9083dup
XR_002956396.1:n.3126+9082_3126+9083dup
NM_000426.4:c.8988+901_8988+902dup MANE Select NP_000417.3:n.8988+901_8988+902dup
NM_001079823.2:c.8976+901_8976+902dup NP_001073291.2:n.8976+901_8976+902dup