Canonical Allele Identifier: CA402044913
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23876324A>G , CM000680.2:g.23876324A>G GRCh38
NC_000018.9:g.21456288A>G , CM000680.1:g.21456288A>G GRCh37
NC_000018.8:g.19710286A>G NCBI36
NG_007853.2:g.191727A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.202A>G MANE Plus Clinical ENSP00000269217.5:p.Lys68Glu
ENST00000313654.14:c.5029A>G MANE Select ENSP00000324532.8:p.Lys1677Glu
ENST00000649721.1:c.1921A>G ENSP00000497885.1:p.Lys641Glu
ENST00000269217.10:c.202A>G ENSP00000269217.5:p.Lys68Glu
ENST00000313654.13:c.5029A>G ENSP00000324532.8:p.Lys1677Glu
ENST00000399516.7:c.5029A>G ENSP00000382432.2:p.Lys1677Glu
ENST00000587184.5:c.202A>G ENSP00000466557.1:p.Lys68Glu
NM_000227.4:c.202A>G NP_000218.3:p.Lys68Glu
NM_001127717.2:c.5029A>G NP_001121189.2:p.Lys1677Glu
NM_001127718.2:c.202A>G NP_001121190.2:p.Lys68Glu
NM_198129.2:c.5029A>G NP_937762.2:p.Lys1677Glu
XM_011525978.1:c.5056A>G XP_011524280.1:p.Lys1686Glu
XM_011525979.1:c.5047A>G XP_011524281.1:p.Lys1683Glu
XM_011525980.1:c.5038A>G XP_011524282.1:p.Lys1680Glu
XM_011525981.1:c.4924A>G XP_011524283.1:p.Lys1642Glu
XM_011525982.1:c.5056A>G XP_011524284.1:p.Lys1686Glu
XM_011525978.2:c.5056A>G XP_011524280.1:p.Lys1686Glu
XM_011525979.2:c.5047A>G XP_011524281.1:p.Lys1683Glu
XM_011525980.2:c.5038A>G XP_011524282.1:p.Lys1680Glu
XM_011525981.2:c.4924A>G XP_011524283.1:p.Lys1642Glu
XM_011525982.2:c.5056A>G XP_011524284.1:p.Lys1686Glu
XM_017025743.1:c.2908A>G XP_016881232.1:p.Lys970Glu
XM_017025744.1:c.598A>G XP_016881233.1:p.Lys200Glu
XR_001753199.1:n.5297A>G
NM_000227.5:c.202A>G NP_000218.3:p.Lys68Glu
NM_001127717.3:c.5029A>G NP_001121189.2:p.Lys1677Glu
NM_001127718.3:c.202A>G NP_001121190.2:p.Lys68Glu
NM_198129.3:c.5029A>G NP_937762.2:p.Lys1677Glu
NM_000227.6:c.202A>G MANE Plus Clinical NP_000218.3:p.Lys68Glu
NM_001127717.4:c.5029A>G NP_001121189.2:p.Lys1677Glu
NM_001127718.4:c.202A>G NP_001121190.2:p.Lys68Glu
NM_198129.4:c.5029A>G MANE Select NP_937762.2:p.Lys1677Glu