Canonical Allele Identifier: CA2290343924
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23949933C= , CM000680.2:g.23949933C= GRCh38
NC_000018.9:g.21529897C= , CM000680.1:g.21529897C= GRCh37
NC_000018.8:g.19783895C= NCBI36
NG_007853.2:g.265336C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.4684+9C= MANE Plus Clinical ENSP00000269217.5:n.4684+9C=
ENST00000313654.14:c.9511+9C= MANE Select ENSP00000324532.8:n.9511+9C=
ENST00000649721.1:c.6106+9C= ENSP00000497885.1:n.6106+9C=
ENST00000269217.10:c.4684+9C= ENSP00000269217.5:n.4684+9C=
ENST00000313654.13:c.9511+9C= ENSP00000324532.8:n.9511+9C=
ENST00000399516.7:c.9343+9C= ENSP00000382432.2:n.9343+9C=
ENST00000587184.5:c.4516+9C= ENSP00000466557.1:n.4516+9C=
ENST00000588004.1:c.32+9C=
ENST00000588770.5:n.4089+9C=
NM_000227.4:c.4684+9C= NP_000218.3:n.4684+9C=
NM_001127717.2:c.9343+9C= NP_001121189.2:n.9343+9C=
NM_001127718.2:c.4516+9C= NP_001121190.2:n.4516+9C=
NM_198129.2:c.9511+9C= NP_937762.2:n.9511+9C=
XM_011525978.1:c.9538+9C= XP_011524280.1:n.9538+9C=
XM_011525979.1:c.9529+9C= XP_011524281.1:n.9529+9C=
XM_011525980.1:c.9520+9C= XP_011524282.1:n.9520+9C=
XM_011525981.1:c.9406+9C= XP_011524283.1:n.9406+9C=
XM_011525982.1:c.9241+9C= XP_011524284.1:n.9241+9C=
XM_011525978.2:c.9538+9C= XP_011524280.1:n.9538+9C=
XM_011525979.2:c.9529+9C= XP_011524281.1:n.9529+9C=
XM_011525980.2:c.9520+9C= XP_011524282.1:n.9520+9C=
XM_011525981.2:c.9406+9C= XP_011524283.1:n.9406+9C=
XM_011525982.2:c.9241+9C= XP_011524284.1:n.9241+9C=
XM_017025743.1:c.7390+9C= XP_016881232.1:n.7390+9C=
XM_017025744.1:c.5080+9C= XP_016881233.1:n.5080+9C=
XR_001753199.1:n.9779+9C=
NM_000227.5:c.4684+9C= NP_000218.3:n.4684+9C=
NM_001127717.3:c.9343+9C= NP_001121189.2:n.9343+9C=
NM_001127718.3:c.4516+9C= NP_001121190.2:n.4516+9C=
NM_198129.3:c.9511+9C= NP_937762.2:n.9511+9C=
NM_000227.6:c.4684+9C= MANE Plus Clinical NP_000218.3:n.4684+9C=
NM_001127717.4:c.9343+9C= NP_001121189.2:n.9343+9C=
NM_001127718.4:c.4516+9C= NP_001121190.2:n.4516+9C=
NM_198129.4:c.9511+9C= MANE Select NP_937762.2:n.9511+9C=