Canonical Allele Identifier: CA1663191533
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129464355G= , CM000668.2:g.129464355G= GRCh38
NC_000006.11:g.129785500G= , CM000668.1:g.129785500G= GRCh37
NC_000006.10:g.129827193G= NCBI36
NG_008678.1:g.586215G= , LRG_409:g.586215G=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.7058G= ENSP00000481744.2:p.Arg2353=
ENST00000618192.5:c.7322G= ENSP00000480802.2:p.Arg2441=
ENST00000684985.1:n.689G=
ENST00000688150.1:n.397G=
ENST00000421865.3:c.7058G= MANE Select ENSP00000400365.2:p.Arg2353=
ENST00000421865.2:c.7058G= ENSP00000400365.2:p.Arg2353=
ENST00000617695.4:c.7058G= ENSP00000481744.1:p.Arg2353=
ENST00000618192.4:c.7055G= ENSP00000480802.1:p.Arg2352=
NM_000426.3:c.7058G= , LRG_409t1:c.7058G= NP_000417.2:p.Arg2353=
NM_001079823.1:c.7058G= NP_001073291.1:p.Arg2353=
XM_005266981.2:c.7322G= XP_005267038.1:p.Arg2441=
XM_005266982.2:c.7322G= XP_005267039.1:p.Arg2441=
XM_011535820.1:c.7316G= XP_011534122.1:p.Arg2439=
XM_005266981.3:c.7322G= XP_005267038.1:p.Arg2441=
XM_005266982.3:c.7322G= XP_005267039.1:p.Arg2441=
XM_011535820.2:c.7316G= XP_011534122.1:p.Arg2439=
XM_017010851.2:c.7328G= XP_016866340.1:p.Arg2443=
XM_017010852.1:c.5453G= XP_016866341.1:p.Arg1818=
NM_000426.4:c.7058G= MANE Select NP_000417.3:p.Arg2353=
NM_001079823.2:c.7058G= NP_001073291.2:p.Arg2353=