Canonical Allele Identifier: CA402051332
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23905551A>T , CM000680.2:g.23905551A>T GRCh38
NC_000018.9:g.21485515A>T , CM000680.1:g.21485515A>T GRCh37
NC_000018.8:g.19739513A>T NCBI36
NG_007853.2:g.220954A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.1818A>T MANE Plus Clinical ENSP00000269217.5:p.Lys606Asn
ENST00000313654.14:c.6645A>T MANE Select ENSP00000324532.8:p.Lys2215Asn
ENST00000649721.1:c.3537A>T ENSP00000497885.1:p.Lys1179Asn
ENST00000269217.10:c.1818A>T ENSP00000269217.5:p.Lys606Asn
ENST00000313654.13:c.6645A>T ENSP00000324532.8:p.Lys2215Asn
ENST00000399516.7:c.6477A>T ENSP00000382432.2:p.Lys2159Asn
ENST00000586751.5:c.1423A>T
ENST00000587184.5:c.1650A>T ENSP00000466557.1:p.Lys550Asn
ENST00000588770.5:n.1223A>T
NM_000227.4:c.1818A>T NP_000218.3:p.Lys606Asn
NM_001127717.2:c.6477A>T NP_001121189.2:p.Lys2159Asn
NM_001127718.2:c.1650A>T NP_001121190.2:p.Lys550Asn
NM_198129.2:c.6645A>T NP_937762.2:p.Lys2215Asn
XM_011525978.1:c.6672A>T XP_011524280.1:p.Lys2224Asn
XM_011525979.1:c.6663A>T XP_011524281.1:p.Lys2221Asn
XM_011525980.1:c.6654A>T XP_011524282.1:p.Lys2218Asn
XM_011525981.1:c.6540A>T XP_011524283.1:p.Lys2180Asn
XM_011525982.1:c.6672A>T XP_011524284.1:p.Lys2224Asn
XM_011525978.2:c.6672A>T XP_011524280.1:p.Lys2224Asn
XM_011525979.2:c.6663A>T XP_011524281.1:p.Lys2221Asn
XM_011525980.2:c.6654A>T XP_011524282.1:p.Lys2218Asn
XM_011525981.2:c.6540A>T XP_011524283.1:p.Lys2180Asn
XM_011525982.2:c.6672A>T XP_011524284.1:p.Lys2224Asn
XM_017025743.1:c.4524A>T XP_016881232.1:p.Lys1508Asn
XM_017025744.1:c.2214A>T XP_016881233.1:p.Lys738Asn
XR_001753199.1:n.6913A>T
NM_000227.5:c.1818A>T NP_000218.3:p.Lys606Asn
NM_001127717.3:c.6477A>T NP_001121189.2:p.Lys2159Asn
NM_001127718.3:c.1650A>T NP_001121190.2:p.Lys550Asn
NM_198129.3:c.6645A>T NP_937762.2:p.Lys2215Asn
NM_000227.6:c.1818A>T MANE Plus Clinical NP_000218.3:p.Lys606Asn
NM_001127717.4:c.6477A>T NP_001121189.2:p.Lys2159Asn
NM_001127718.4:c.1650A>T NP_001121190.2:p.Lys550Asn
NM_198129.4:c.6645A>T MANE Select NP_937762.2:p.Lys2215Asn