Canonical Allele Identifier: CA2290328868
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23915234_23915235delinsAT , CM000680.2:g.23915234_23915235delinsAT GRCh38
NC_000018.9:g.21495198_21495199delinsAT , CM000680.1:g.21495198_21495199delinsAT GRCh37
NC_000018.8:g.19749196_19749197delinsAT NCBI36
NG_007853.2:g.230637_230638delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.2818-55_2818-54delinsAT MANE Plus Clinical ENSP00000269217.5:n.2818-55_2818-54delins...
ENST00000313654.14:c.7645-55_7645-54delinsAT MANE Select ENSP00000324532.8:n.7645-55_7645-54delins...
ENST00000649721.1:c.4240-55_4240-54delinsAT ENSP00000497885.1:n.4240-55_4240-54delins...
ENST00000269217.10:c.2818-55_2818-54delinsAT ENSP00000269217.5:n.2818-55_2818-54delins...
ENST00000313654.13:c.7645-55_7645-54delinsAT ENSP00000324532.8:n.7645-55_7645-54delins...
ENST00000399516.7:c.7477-55_7477-54delinsAT ENSP00000382432.2:n.7477-55_7477-54delins...
ENST00000586751.5:c.2423-55_2423-54delinsAT
ENST00000587184.5:c.2650-55_2650-54delinsAT ENSP00000466557.1:n.2650-55_2650-54delins...
ENST00000588770.5:n.2223-55_2223-54delinsAT
NM_000227.4:c.2818-55_2818-54delinsAT NP_000218.3:n.2818-55_2818-54delinsAT
NM_001127717.2:c.7477-55_7477-54delinsAT NP_001121189.2:n.7477-55_7477-54delinsAT
NM_001127718.2:c.2650-55_2650-54delinsAT NP_001121190.2:n.2650-55_2650-54delinsAT
NM_198129.2:c.7645-55_7645-54delinsAT NP_937762.2:n.7645-55_7645-54delinsAT
XM_011525978.1:c.7672-55_7672-54delinsAT XP_011524280.1:n.7672-55_7672-54delinsAT
XM_011525979.1:c.7663-55_7663-54delinsAT XP_011524281.1:n.7663-55_7663-54delinsAT
XM_011525980.1:c.7654-55_7654-54delinsAT XP_011524282.1:n.7654-55_7654-54delinsAT
XM_011525981.1:c.7540-55_7540-54delinsAT XP_011524283.1:n.7540-55_7540-54delinsAT
XM_011525982.1:c.7375-55_7375-54delinsAT XP_011524284.1:n.7375-55_7375-54delinsAT
XM_011525978.2:c.7672-55_7672-54delinsAT XP_011524280.1:n.7672-55_7672-54delinsAT
XM_011525979.2:c.7663-55_7663-54delinsAT XP_011524281.1:n.7663-55_7663-54delinsAT
XM_011525980.2:c.7654-55_7654-54delinsAT XP_011524282.1:n.7654-55_7654-54delinsAT
XM_011525981.2:c.7540-55_7540-54delinsAT XP_011524283.1:n.7540-55_7540-54delinsAT
XM_011525982.2:c.7375-55_7375-54delinsAT XP_011524284.1:n.7375-55_7375-54delinsAT
XM_017025743.1:c.5524-55_5524-54delinsAT XP_016881232.1:n.5524-55_5524-54delinsAT
XM_017025744.1:c.3214-55_3214-54delinsAT XP_016881233.1:n.3214-55_3214-54delinsAT
XR_001753199.1:n.7913-55_7913-54delinsAT
NM_000227.5:c.2818-55_2818-54delinsAT NP_000218.3:n.2818-55_2818-54delinsAT
NM_001127717.3:c.7477-55_7477-54delinsAT NP_001121189.2:n.7477-55_7477-54delinsAT
NM_001127718.3:c.2650-55_2650-54delinsAT NP_001121190.2:n.2650-55_2650-54delinsAT
NM_198129.3:c.7645-55_7645-54delinsAT NP_937762.2:n.7645-55_7645-54delinsAT
NM_000227.6:c.2818-55_2818-54delinsAT MANE Plus Clinical NP_000218.3:n.2818-55_2818-54delinsAT
NM_001127717.4:c.7477-55_7477-54delinsAT NP_001121189.2:n.7477-55_7477-54delinsAT
NM_001127718.4:c.2650-55_2650-54delinsAT NP_001121190.2:n.2650-55_2650-54delinsAT
NM_198129.4:c.7645-55_7645-54delinsAT MANE Select NP_937762.2:n.7645-55_7645-54delinsAT