Canonical Allele Identifier: CA2290323875
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23903006C= , CM000680.2:g.23903006C= GRCh38
NC_000018.9:g.21482970C= , CM000680.1:g.21482970C= GRCh37
NC_000018.8:g.19736968C= NCBI36
NG_007853.2:g.218409C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.1375-3C= MANE Plus Clinical ENSP00000269217.5:n.1375-3C=
ENST00000313654.14:c.6202-3C= MANE Select ENSP00000324532.8:n.6202-3C=
ENST00000649721.1:c.3094-3C= ENSP00000497885.1:n.3094-3C=
ENST00000269217.10:c.1375-3C= ENSP00000269217.5:n.1375-3C=
ENST00000313654.13:c.6202-3C= ENSP00000324532.8:n.6202-3C=
ENST00000399516.7:c.6034-3C= ENSP00000382432.2:n.6034-3C=
ENST00000586751.5:c.980-3C=
ENST00000587184.5:c.1207-3C= ENSP00000466557.1:n.1207-3C=
ENST00000588770.5:n.780-3C=
NM_000227.4:c.1375-3C= NP_000218.3:n.1375-3C=
NM_001127717.2:c.6034-3C= NP_001121189.2:n.6034-3C=
NM_001127718.2:c.1207-3C= NP_001121190.2:n.1207-3C=
NM_198129.2:c.6202-3C= NP_937762.2:n.6202-3C=
XM_011525978.1:c.6229-3C= XP_011524280.1:n.6229-3C=
XM_011525979.1:c.6220-3C= XP_011524281.1:n.6220-3C=
XM_011525980.1:c.6211-3C= XP_011524282.1:n.6211-3C=
XM_011525981.1:c.6097-3C= XP_011524283.1:n.6097-3C=
XM_011525982.1:c.6229-3C= XP_011524284.1:n.6229-3C=
XM_011525978.2:c.6229-3C= XP_011524280.1:n.6229-3C=
XM_011525979.2:c.6220-3C= XP_011524281.1:n.6220-3C=
XM_011525980.2:c.6211-3C= XP_011524282.1:n.6211-3C=
XM_011525981.2:c.6097-3C= XP_011524283.1:n.6097-3C=
XM_011525982.2:c.6229-3C= XP_011524284.1:n.6229-3C=
XM_017025743.1:c.4081-3C= XP_016881232.1:n.4081-3C=
XM_017025744.1:c.1771-3C= XP_016881233.1:n.1771-3C=
XR_001753199.1:n.6470-3C=
NM_000227.5:c.1375-3C= NP_000218.3:n.1375-3C=
NM_001127717.3:c.6034-3C= NP_001121189.2:n.6034-3C=
NM_001127718.3:c.1207-3C= NP_001121190.2:n.1207-3C=
NM_198129.3:c.6202-3C= NP_937762.2:n.6202-3C=
NM_000227.6:c.1375-3C= MANE Plus Clinical NP_000218.3:n.1375-3C=
NM_001127717.4:c.6034-3C= NP_001121189.2:n.6034-3C=
NM_001127718.4:c.1207-3C= NP_001121190.2:n.1207-3C=
NM_198129.4:c.6202-3C= MANE Select NP_937762.2:n.6202-3C=