Canonical Allele Identifier: CA1663191538
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129464356T= , CM000668.2:g.129464356T= GRCh38
NC_000006.11:g.129785501T= , CM000668.1:g.129785501T= GRCh37
NC_000006.10:g.129827194T= NCBI36
NG_008678.1:g.586216T= , LRG_409:g.586216T=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.7059T= ENSP00000481744.2:p.Arg2353=
ENST00000618192.5:c.7323T= ENSP00000480802.2:p.Arg2441=
ENST00000684985.1:n.690T=
ENST00000688150.1:n.398T=
ENST00000421865.3:c.7059T= MANE Select ENSP00000400365.2:p.Arg2353=
ENST00000421865.2:c.7059T= ENSP00000400365.2:p.Arg2353=
ENST00000617695.4:c.7059T= ENSP00000481744.1:p.Arg2353=
ENST00000618192.4:c.7056T= ENSP00000480802.1:p.Arg2352=
NM_000426.3:c.7059T= , LRG_409t1:c.7059T= NP_000417.2:p.Arg2353=
NM_001079823.1:c.7059T= NP_001073291.1:p.Arg2353=
XM_005266981.2:c.7323T= XP_005267038.1:p.Arg2441=
XM_005266982.2:c.7323T= XP_005267039.1:p.Arg2441=
XM_011535820.1:c.7317T= XP_011534122.1:p.Arg2439=
XM_005266981.3:c.7323T= XP_005267038.1:p.Arg2441=
XM_005266982.3:c.7323T= XP_005267039.1:p.Arg2441=
XM_011535820.2:c.7317T= XP_011534122.1:p.Arg2439=
XM_017010851.2:c.7329T= XP_016866340.1:p.Arg2443=
XM_017010852.1:c.5454T= XP_016866341.1:p.Arg1818=
NM_000426.4:c.7059T= MANE Select NP_000417.3:p.Arg2353=
NM_001079823.2:c.7059T= NP_001073291.2:p.Arg2353=