Canonical Allele Identifier: CA2290343973
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23949982T= , CM000680.2:g.23949982T= GRCh38
NC_000018.9:g.21529946T= , CM000680.1:g.21529946T= GRCh37
NC_000018.8:g.19783944T= NCBI36
NG_007853.2:g.265385T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.4685-47T= MANE Plus Clinical ENSP00000269217.5:n.4685-47T=
ENST00000313654.14:c.9512-47T= MANE Select ENSP00000324532.8:n.9512-47T=
ENST00000649721.1:c.6107-47T= ENSP00000497885.1:n.6107-47T=
ENST00000269217.10:c.4685-47T= ENSP00000269217.5:n.4685-47T=
ENST00000313654.13:c.9512-47T= ENSP00000324532.8:n.9512-47T=
ENST00000399516.7:c.9344-47T= ENSP00000382432.2:n.9344-47T=
ENST00000587184.5:c.4517-47T= ENSP00000466557.1:n.4517-47T=
ENST00000588004.1:c.33-47T=
ENST00000588770.5:n.4090-47T=
NM_000227.4:c.4685-47T= NP_000218.3:n.4685-47T=
NM_001127717.2:c.9344-47T= NP_001121189.2:n.9344-47T=
NM_001127718.2:c.4517-47T= NP_001121190.2:n.4517-47T=
NM_198129.2:c.9512-47T= NP_937762.2:n.9512-47T=
XM_011525978.1:c.9539-47T= XP_011524280.1:n.9539-47T=
XM_011525979.1:c.9530-47T= XP_011524281.1:n.9530-47T=
XM_011525980.1:c.9521-47T= XP_011524282.1:n.9521-47T=
XM_011525981.1:c.9407-47T= XP_011524283.1:n.9407-47T=
XM_011525982.1:c.9242-47T= XP_011524284.1:n.9242-47T=
XM_011525978.2:c.9539-47T= XP_011524280.1:n.9539-47T=
XM_011525979.2:c.9530-47T= XP_011524281.1:n.9530-47T=
XM_011525980.2:c.9521-47T= XP_011524282.1:n.9521-47T=
XM_011525981.2:c.9407-47T= XP_011524283.1:n.9407-47T=
XM_011525982.2:c.9242-47T= XP_011524284.1:n.9242-47T=
XM_017025743.1:c.7391-47T= XP_016881232.1:n.7391-47T=
XM_017025744.1:c.5081-47T= XP_016881233.1:n.5081-47T=
XR_001753199.1:n.9780-47T=
NM_000227.5:c.4685-47T= NP_000218.3:n.4685-47T=
NM_001127717.3:c.9344-47T= NP_001121189.2:n.9344-47T=
NM_001127718.3:c.4517-47T= NP_001121190.2:n.4517-47T=
NM_198129.3:c.9512-47T= NP_937762.2:n.9512-47T=
NM_000227.6:c.4685-47T= MANE Plus Clinical NP_000218.3:n.4685-47T=
NM_001127717.4:c.9344-47T= NP_001121189.2:n.9344-47T=
NM_001127718.4:c.4517-47T= NP_001121190.2:n.4517-47T=
NM_198129.4:c.9512-47T= MANE Select NP_937762.2:n.9512-47T=