Canonical Allele Identifier: CA1663191515
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129464348G= , CM000668.2:g.129464348G= GRCh38
NC_000006.11:g.129785493G= , CM000668.1:g.129785493G= GRCh37
NC_000006.10:g.129827186G= NCBI36
NG_008678.1:g.586208G= , LRG_409:g.586208G=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.7051G= ENSP00000481744.2:p.Val2351=
ENST00000618192.5:c.7315G= ENSP00000480802.2:p.Val2439=
ENST00000684985.1:n.682G=
ENST00000688150.1:n.390G=
ENST00000421865.3:c.7051G= MANE Select ENSP00000400365.2:p.Val2351=
ENST00000421865.2:c.7051G= ENSP00000400365.2:p.Val2351=
ENST00000617695.4:c.7051G= ENSP00000481744.1:p.Val2351=
ENST00000618192.4:c.7048G= ENSP00000480802.1:p.Val2350=
NM_000426.3:c.7051G= , LRG_409t1:c.7051G= NP_000417.2:p.Val2351=
NM_001079823.1:c.7051G= NP_001073291.1:p.Val2351=
XM_005266981.2:c.7315G= XP_005267038.1:p.Val2439=
XM_005266982.2:c.7315G= XP_005267039.1:p.Val2439=
XM_011535820.1:c.7309G= XP_011534122.1:p.Val2437=
XM_005266981.3:c.7315G= XP_005267038.1:p.Val2439=
XM_005266982.3:c.7315G= XP_005267039.1:p.Val2439=
XM_011535820.2:c.7309G= XP_011534122.1:p.Val2437=
XM_017010851.2:c.7321G= XP_016866340.1:p.Val2441=
XM_017010852.1:c.5446G= XP_016866341.1:p.Val1816=
NM_000426.4:c.7051G= MANE Select NP_000417.3:p.Val2351=
NM_001079823.2:c.7051G= NP_001073291.2:p.Val2351=