Canonical Allele Identifier: CA1663161497
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129427753C= , CM000668.2:g.129427753C= GRCh38
NC_000006.11:g.129748898C= , CM000668.1:g.129748898C= GRCh37
NC_000006.10:g.129790591C= NCBI36
NG_008678.1:g.549613C= , LRG_409:g.549613C=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.5867C= ENSP00000481744.2:p.Ala1956=
ENST00000618192.5:c.6131C= ENSP00000480802.2:p.Ala2044=
ENST00000421865.3:c.5867C= MANE Select ENSP00000400365.2:p.Ala1956=
ENST00000421865.2:c.5867C= ENSP00000400365.2:p.Ala1956=
ENST00000617695.4:c.5867C= ENSP00000481744.1:p.Ala1956=
ENST00000618192.4:c.5867C= ENSP00000480802.1:p.Ala1956=
NM_000426.3:c.5867C= , LRG_409t1:c.5867C= NP_000417.2:p.Ala1956=
NM_001079823.1:c.5867C= NP_001073291.1:p.Ala1956=
XM_005266981.2:c.6131C= XP_005267038.1:p.Ala2044=
XM_005266982.2:c.6131C= XP_005267039.1:p.Ala2044=
XM_011535820.1:c.6131C= XP_011534122.1:p.Ala2044=
XM_005266981.3:c.6131C= XP_005267038.1:p.Ala2044=
XM_005266982.3:c.6131C= XP_005267039.1:p.Ala2044=
XM_011535820.2:c.6131C= XP_011534122.1:p.Ala2044=
XM_017010851.2:c.6137C= XP_016866340.1:p.Ala2046=
XM_017010852.1:c.4262C= XP_016866341.1:p.Ala1421=
NM_000426.4:c.5867C= MANE Select NP_000417.3:p.Ala1956=
NM_001079823.2:c.5867C= NP_001073291.2:p.Ala1956=