Canonical Allele Identifier: CA1663078503
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129314704G= , CM000668.2:g.129314704G= GRCh38
NC_000006.11:g.129635849G= , CM000668.1:g.129635849G= GRCh37
NC_000006.10:g.129677542G= NCBI36
NG_008678.1:g.436564G= , LRG_409:g.436564G=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.3461G= ENSP00000481744.2:p.Gly1154=
ENST00000618192.5:c.3725G= ENSP00000480802.2:p.Gly1242=
ENST00000421865.3:c.3461G= MANE Select ENSP00000400365.2:p.Gly1154=
ENST00000421865.2:c.3461G= ENSP00000400365.2:p.Gly1154=
ENST00000617695.4:c.3461G= ENSP00000481744.1:p.Gly1154=
ENST00000618192.4:c.3461G= ENSP00000480802.1:p.Gly1154=
NM_000426.3:c.3461G= , LRG_409t1:c.3461G= NP_000417.2:p.Gly1154=
NM_001079823.1:c.3461G= NP_001073291.1:p.Gly1154=
XM_005266981.2:c.3725G= XP_005267038.1:p.Gly1242=
XM_005266982.2:c.3725G= XP_005267039.1:p.Gly1242=
XM_011535820.1:c.3725G= XP_011534122.1:p.Gly1242=
XM_005266981.3:c.3725G= XP_005267038.1:p.Gly1242=
XM_005266982.3:c.3725G= XP_005267039.1:p.Gly1242=
XM_011535820.2:c.3725G= XP_011534122.1:p.Gly1242=
XM_017010851.2:c.3731G= XP_016866340.1:p.Gly1244=
XM_017010852.1:c.1856G= XP_016866341.1:p.Gly619=
XM_017010853.1:c.3725G= XP_016866342.1:p.Gly1242=
NM_000426.4:c.3461G= MANE Select NP_000417.3:p.Gly1154=
NM_001079823.2:c.3461G= NP_001073291.2:p.Gly1154=