Canonical Allele Identifier: CA402044870
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23876303C>T , CM000680.2:g.23876303C>T GRCh38
NC_000018.9:g.21456267C>T , CM000680.1:g.21456267C>T GRCh37
NC_000018.8:g.19710265C>T NCBI36
NG_007853.2:g.191706C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.181C>T MANE Plus Clinical ENSP00000269217.5:p.Pro61Ser
ENST00000313654.14:c.5008C>T MANE Select ENSP00000324532.8:p.Pro1670Ser
ENST00000649721.1:c.1900C>T ENSP00000497885.1:p.Pro634Ser
ENST00000269217.10:c.181C>T ENSP00000269217.5:p.Pro61Ser
ENST00000313654.13:c.5008C>T ENSP00000324532.8:p.Pro1670Ser
ENST00000399516.7:c.5008C>T ENSP00000382432.2:p.Pro1670Ser
ENST00000587184.5:c.181C>T ENSP00000466557.1:p.Pro61Ser
NM_000227.4:c.181C>T NP_000218.3:p.Pro61Ser
NM_001127717.2:c.5008C>T NP_001121189.2:p.Pro1670Ser
NM_001127718.2:c.181C>T NP_001121190.2:p.Pro61Ser
NM_198129.2:c.5008C>T NP_937762.2:p.Pro1670Ser
XM_011525978.1:c.5035C>T XP_011524280.1:p.Pro1679Ser
XM_011525979.1:c.5026C>T XP_011524281.1:p.Pro1676Ser
XM_011525980.1:c.5017C>T XP_011524282.1:p.Pro1673Ser
XM_011525981.1:c.4903C>T XP_011524283.1:p.Pro1635Ser
XM_011525982.1:c.5035C>T XP_011524284.1:p.Pro1679Ser
XM_011525978.2:c.5035C>T XP_011524280.1:p.Pro1679Ser
XM_011525979.2:c.5026C>T XP_011524281.1:p.Pro1676Ser
XM_011525980.2:c.5017C>T XP_011524282.1:p.Pro1673Ser
XM_011525981.2:c.4903C>T XP_011524283.1:p.Pro1635Ser
XM_011525982.2:c.5035C>T XP_011524284.1:p.Pro1679Ser
XM_017025743.1:c.2887C>T XP_016881232.1:p.Pro963Ser
XM_017025744.1:c.577C>T XP_016881233.1:p.Pro193Ser
XR_001753199.1:n.5276C>T
NM_000227.5:c.181C>T NP_000218.3:p.Pro61Ser
NM_001127717.3:c.5008C>T NP_001121189.2:p.Pro1670Ser
NM_001127718.3:c.181C>T NP_001121190.2:p.Pro61Ser
NM_198129.3:c.5008C>T NP_937762.2:p.Pro1670Ser
NM_000227.6:c.181C>T MANE Plus Clinical NP_000218.3:p.Pro61Ser
NM_001127717.4:c.5008C>T NP_001121189.2:p.Pro1670Ser
NM_001127718.4:c.181C>T NP_001121190.2:p.Pro61Ser
NM_198129.4:c.5008C>T MANE Select NP_937762.2:p.Pro1670Ser