Canonical Allele Identifier: CA242505
Gene: LAMA2 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129315505A>G , CM000668.2:g.129315505A>G GRCh38
NC_000006.11:g.129636650A>G , CM000668.1:g.129636650A>G GRCh37
NC_000006.10:g.129678343A>G NCBI36
NG_008678.1:g.437365A>G , LRG_409:g.437365A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000617695.5:c.3585A>G ENSP00000481744.2:p.Leu1195=
ENST00000618192.5:c.3849A>G ENSP00000480802.2:p.Leu1283=
ENST00000421865.3:c.3585A>G MANE Select ENSP00000400365.2:p.Leu1195=
ENST00000421865.2:c.3585A>G ENSP00000400365.2:p.Leu1195=
ENST00000617695.4:c.3585A>G ENSP00000481744.1:p.Leu1195=
ENST00000618192.4:c.3585A>G ENSP00000480802.1:p.Leu1195=
NM_000426.3:c.3585A>G , LRG_409t1:c.3585A>G NP_000417.2:p.Leu1195=
NM_001079823.1:c.3585A>G NP_001073291.1:p.Leu1195=
XM_005266981.2:c.3849A>G XP_005267038.1:p.Leu1283=
XM_005266982.2:c.3849A>G XP_005267039.1:p.Leu1283=
XM_011535820.1:c.3849A>G XP_011534122.1:p.Leu1283=
XM_005266981.3:c.3849A>G XP_005267038.1:p.Leu1283=
XM_005266982.3:c.3849A>G XP_005267039.1:p.Leu1283=
XM_011535820.2:c.3849A>G XP_011534122.1:p.Leu1283=
XM_017010851.2:c.3855A>G XP_016866340.1:p.Leu1285=
XM_017010852.1:c.1980A>G XP_016866341.1:p.Leu660=
XM_017010853.1:c.3849A>G XP_016866342.1:p.Leu1283=
NM_000426.4:c.3585A>G MANE Select NP_000417.3:p.Leu1195=
NM_001079823.2:c.3585A>G NP_001073291.2:p.Leu1195=