Canonical Allele Identifier: CA1663173812
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129481390G= , CM000668.2:g.129481390G= GRCh38
NC_000006.11:g.129802535G= , CM000668.1:g.129802535G= GRCh37
NC_000006.10:g.129844228G= NCBI36
NG_008678.1:g.603250G= , LRG_409:g.603250G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617695.5:c.7688G= ENSP00000481744.2:p.Ser2563=
ENST00000618192.5:c.7964G= ENSP00000480802.2:p.Ser2655=
ENST00000421865.3:c.7700G= MANE Select ENSP00000400365.2:p.Ser2567=
ENST00000421865.2:c.7700G= ENSP00000400365.2:p.Ser2567=
ENST00000617695.4:c.7688G= ENSP00000481744.1:p.Ser2563=
ENST00000618192.4:c.7697G= ENSP00000480802.1:p.Ser2566=
NM_000426.3:c.7700G= , LRG_409t1:c.7700G= NP_000417.2:p.Ser2567=
NM_001079823.1:c.7688G= NP_001073291.1:p.Ser2563=
XM_005266981.2:c.7964G= XP_005267038.1:p.Ser2655=
XM_005266982.2:c.7952G= XP_005267039.1:p.Ser2651=
XM_011535820.1:c.7958G= XP_011534122.1:p.Ser2653=
XM_005266981.3:c.7964G= XP_005267038.1:p.Ser2655=
XM_005266982.3:c.7952G= XP_005267039.1:p.Ser2651=
XM_011535820.2:c.7958G= XP_011534122.1:p.Ser2653=
XM_017010851.2:c.7970G= XP_016866340.1:p.Ser2657=
XM_017010852.1:c.6095G= XP_016866341.1:p.Ser2032=
NM_000426.4:c.7700G= MANE Select NP_000417.3:p.Ser2567=
NM_001079823.2:c.7688G= NP_001073291.2:p.Ser2563=