Canonical Allele Identifier: CA402048711
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23903037A>C , CM000680.2:g.23903037A>C GRCh38
NC_000018.9:g.21483001A>C , CM000680.1:g.21483001A>C GRCh37
NC_000018.8:g.19736999A>C NCBI36
NG_007853.2:g.218440A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.1403A>C MANE Plus Clinical ENSP00000269217.5:p.Gln468Pro
ENST00000313654.14:c.6230A>C MANE Select ENSP00000324532.8:p.Gln2077Pro
ENST00000649721.1:c.3122A>C ENSP00000497885.1:p.Gln1041Pro
ENST00000269217.10:c.1403A>C ENSP00000269217.5:p.Gln468Pro
ENST00000313654.13:c.6230A>C ENSP00000324532.8:p.Gln2077Pro
ENST00000399516.7:c.6062A>C ENSP00000382432.2:p.Gln2021Pro
ENST00000586751.5:c.1008A>C
ENST00000587184.5:c.1235A>C ENSP00000466557.1:p.Gln412Pro
ENST00000588770.5:n.808A>C
NM_000227.4:c.1403A>C NP_000218.3:p.Gln468Pro
NM_001127717.2:c.6062A>C NP_001121189.2:p.Gln2021Pro
NM_001127718.2:c.1235A>C NP_001121190.2:p.Gln412Pro
NM_198129.2:c.6230A>C NP_937762.2:p.Gln2077Pro
XM_011525978.1:c.6257A>C XP_011524280.1:p.Gln2086Pro
XM_011525979.1:c.6248A>C XP_011524281.1:p.Gln2083Pro
XM_011525980.1:c.6239A>C XP_011524282.1:p.Gln2080Pro
XM_011525981.1:c.6125A>C XP_011524283.1:p.Gln2042Pro
XM_011525982.1:c.6257A>C XP_011524284.1:p.Gln2086Pro
XM_011525978.2:c.6257A>C XP_011524280.1:p.Gln2086Pro
XM_011525979.2:c.6248A>C XP_011524281.1:p.Gln2083Pro
XM_011525980.2:c.6239A>C XP_011524282.1:p.Gln2080Pro
XM_011525981.2:c.6125A>C XP_011524283.1:p.Gln2042Pro
XM_011525982.2:c.6257A>C XP_011524284.1:p.Gln2086Pro
XM_017025743.1:c.4109A>C XP_016881232.1:p.Gln1370Pro
XM_017025744.1:c.1799A>C XP_016881233.1:p.Gln600Pro
XR_001753199.1:n.6498A>C
NM_000227.5:c.1403A>C NP_000218.3:p.Gln468Pro
NM_001127717.3:c.6062A>C NP_001121189.2:p.Gln2021Pro
NM_001127718.3:c.1235A>C NP_001121190.2:p.Gln412Pro
NM_198129.3:c.6230A>C NP_937762.2:p.Gln2077Pro
NM_000227.6:c.1403A>C MANE Plus Clinical NP_000218.3:p.Gln468Pro
NM_001127717.4:c.6062A>C NP_001121189.2:p.Gln2021Pro
NM_001127718.4:c.1235A>C NP_001121190.2:p.Gln412Pro
NM_198129.4:c.6230A>C MANE Select NP_937762.2:p.Gln2077Pro