Canonical Allele Identifier: CA1663191505
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129464344A= , CM000668.2:g.129464344A= GRCh38
NC_000006.11:g.129785489A= , CM000668.1:g.129785489A= GRCh37
NC_000006.10:g.129827182A= NCBI36
NG_008678.1:g.586204A= , LRG_409:g.586204A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617695.5:c.7047A= ENSP00000481744.2:p.Ala2349=
ENST00000618192.5:c.7311A= ENSP00000480802.2:p.Ala2437=
ENST00000684985.1:n.678A=
ENST00000688150.1:n.386A=
ENST00000421865.3:c.7047A= MANE Select ENSP00000400365.2:p.Ala2349=
ENST00000421865.2:c.7047A= ENSP00000400365.2:p.Ala2349=
ENST00000617695.4:c.7047A= ENSP00000481744.1:p.Ala2349=
ENST00000618192.4:c.7044A= ENSP00000480802.1:p.Ala2348=
NM_000426.3:c.7047A= , LRG_409t1:c.7047A= NP_000417.2:p.Ala2349=
NM_001079823.1:c.7047A= NP_001073291.1:p.Ala2349=
XM_005266981.2:c.7311A= XP_005267038.1:p.Ala2437=
XM_005266982.2:c.7311A= XP_005267039.1:p.Ala2437=
XM_011535820.1:c.7305A= XP_011534122.1:p.Ala2435=
XM_005266981.3:c.7311A= XP_005267038.1:p.Ala2437=
XM_005266982.3:c.7311A= XP_005267039.1:p.Ala2437=
XM_011535820.2:c.7305A= XP_011534122.1:p.Ala2435=
XM_017010851.2:c.7317A= XP_016866340.1:p.Ala2439=
XM_017010852.1:c.5442A= XP_016866341.1:p.Ala1814=
NM_000426.4:c.7047A= MANE Select NP_000417.3:p.Ala2349=
NM_001079823.2:c.7047A= NP_001073291.2:p.Ala2349=