Canonical Allele Identifier: CA1663080101
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129315638C= , CM000668.2:g.129315638C= GRCh38
NC_000006.11:g.129636783C= , CM000668.1:g.129636783C= GRCh37
NC_000006.10:g.129678476C= NCBI36
NG_008678.1:g.437498C= , LRG_409:g.437498C=

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.3718C= ENSP00000481744.2:p.Gln1240=
ENST00000618192.5:c.3982C= ENSP00000480802.2:p.Gln1328=
ENST00000421865.3:c.3718C= MANE Select ENSP00000400365.2:p.Gln1240=
ENST00000421865.2:c.3718C= ENSP00000400365.2:p.Gln1240=
ENST00000617695.4:c.3718C= ENSP00000481744.1:p.Gln1240=
ENST00000618192.4:c.3718C= ENSP00000480802.1:p.Gln1240=
NM_000426.3:c.3718C= , LRG_409t1:c.3718C= NP_000417.2:p.Gln1240=
NM_001079823.1:c.3718C= NP_001073291.1:p.Gln1240=
XM_005266981.2:c.3982C= XP_005267038.1:p.Gln1328=
XM_005266982.2:c.3982C= XP_005267039.1:p.Gln1328=
XM_011535820.1:c.3982C= XP_011534122.1:p.Gln1328=
XM_005266981.3:c.3982C= XP_005267038.1:p.Gln1328=
XM_005266982.3:c.3982C= XP_005267039.1:p.Gln1328=
XM_011535820.2:c.3982C= XP_011534122.1:p.Gln1328=
XM_017010851.2:c.3988C= XP_016866340.1:p.Gln1330=
XM_017010852.1:c.2113C= XP_016866341.1:p.Gln705=
XM_017010853.1:c.3982C= XP_016866342.1:p.Gln1328=
NM_000426.4:c.3718C= MANE Select NP_000417.3:p.Gln1240=
NM_001079823.2:c.3718C= NP_001073291.2:p.Gln1240=