Canonical Allele Identifier: CA220810
Gene: LAMA2 HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129146969C>T , CM000668.2:g.129146969C>T GRCh38
NC_000006.11:g.129468114C>T , CM000668.1:g.129468114C>T GRCh37
NC_000006.10:g.129509807C>T NCBI36
NG_008678.1:g.268829C>T , LRG_409:g.268829C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000617695.5:c.830C>T ENSP00000481744.2:p.Ser277Leu
ENST00000618192.5:c.830C>T ENSP00000480802.2:p.Ser277Leu
ENST00000685128.1:n.359C>T
ENST00000686577.1:n.896C>T
ENST00000686599.1:n.935C>T
ENST00000690881.1:n.293C>T
ENST00000421865.3:c.830C>T MANE Select ENSP00000400365.2:p.Ser277Leu
ENST00000421865.2:c.830C>T ENSP00000400365.2:p.Ser277Leu
ENST00000617695.4:c.830C>T ENSP00000481744.1:p.Ser277Leu
ENST00000618192.4:c.830C>T ENSP00000480802.1:p.Ser277Leu
NM_000426.3:c.830C>T , LRG_409t1:c.830C>T NP_000417.2:p.Ser277Leu
NM_001079823.1:c.830C>T NP_001073291.1:p.Ser277Leu
XM_005266981.2:c.830C>T XP_005267038.1:p.Ser277Leu
XM_005266982.2:c.830C>T XP_005267039.1:p.Ser277Leu
XM_011535820.1:c.830C>T XP_011534122.1:p.Ser277Leu
XM_005266981.3:c.830C>T XP_005267038.1:p.Ser277Leu
XM_005266982.3:c.830C>T XP_005267039.1:p.Ser277Leu
XM_011535820.2:c.830C>T XP_011534122.1:p.Ser277Leu
XM_017010851.2:c.836C>T XP_016866340.1:p.Ser279Leu
XM_017010853.1:c.830C>T XP_016866342.1:p.Ser277Leu
NM_000426.4:c.830C>T MANE Select NP_000417.3:p.Ser277Leu
NM_001079823.2:c.830C>T NP_001073291.2:p.Ser277Leu