Canonical Allele Identifier: CA3994444
Community Standard Title: NM_000426.4(LAMA2):c.7118C>T (p.Ser2373Leu)
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129464415C>T , CM000668.2:g.129464415C>T GRCh38
NC_000006.11:g.129785560C>T , CM000668.1:g.129785560C>T GRCh37
NC_000006.10:g.129827253C>T NCBI36
NG_008678.1:g.586275C>T , LRG_409:g.586275C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000426.4:c.7118C>T MANE Select NP_000417.3:p.Ser2373Leu
ENST00000421865.3:c.7118C>T MANE Select ENSP00000400365.2:p.Ser2373Leu
NM_000426.3:c.7118C>T , LRG_409t1:c.7118C>T NP_000417.2:p.Ser2373Leu
NM_001079823.1:c.7118C>T NP_001073291.1:p.Ser2373Leu
NM_001079823.2:c.7118C>T NP_001073291.2:p.Ser2373Leu
ENST00000421865.2:c.7118C>T ENSP00000400365.2:p.Ser2373Leu
ENST00000617695.4:c.7118C>T ENSP00000481744.1:p.Ser2373Leu
ENST00000617695.5:c.7118C>T ENSP00000481744.2:p.Ser2373Leu
ENST00000618192.4:c.7115C>T ENSP00000480802.1:p.Ser2372Leu
ENST00000618192.5:c.7382C>T ENSP00000480802.2:p.Ser2461Leu
ENST00000684985.1:n.749C>T
ENST00000688150.1:n.457C>T
XM_005266981.2:c.7382C>T XP_005267038.1:p.Ser2461Leu
XM_005266981.3:c.7382C>T XP_005267038.1:p.Ser2461Leu
XM_005266982.2:c.7382C>T XP_005267039.1:p.Ser2461Leu
XM_005266982.3:c.7382C>T XP_005267039.1:p.Ser2461Leu
XM_011535820.1:c.7376C>T XP_011534122.1:p.Ser2459Leu
XM_011535820.2:c.7376C>T XP_011534122.1:p.Ser2459Leu
XM_017010851.2:c.7388C>T XP_016866340.1:p.Ser2463Leu
XM_017010852.1:c.5513C>T XP_016866341.1:p.Ser1838Leu