Canonical Allele Identifier: CA2290343953
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23949959_23949960delinsAT , CM000680.2:g.23949959_23949960delinsAT GRCh38
NC_000018.9:g.21529923_21529924delinsAT , CM000680.1:g.21529923_21529924delinsAT GRCh37
NC_000018.8:g.19783921_19783922delinsAT NCBI36
NG_007853.2:g.265362_265363delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.4684+35_4684+36delinsAT MANE Plus Clinical ENSP00000269217.5:n.4684+35_4684+36delinsAT
ENST00000313654.14:c.9511+35_9511+36delinsAT MANE Select ENSP00000324532.8:n.9511+35_9511+36delinsAT
ENST00000649721.1:c.6106+35_6106+36delinsAT ENSP00000497885.1:n.6106+35_6106+36delinsAT
ENST00000269217.10:c.4684+35_4684+36delinsAT ENSP00000269217.5:n.4684+35_4684+36delinsAT
ENST00000313654.13:c.9511+35_9511+36delinsAT ENSP00000324532.8:n.9511+35_9511+36delinsAT
ENST00000399516.7:c.9343+35_9343+36delinsAT ENSP00000382432.2:n.9343+35_9343+36delinsAT
ENST00000587184.5:c.4516+35_4516+36delinsAT ENSP00000466557.1:n.4516+35_4516+36delinsAT
ENST00000588004.1:c.32+35_32+36delinsAT
ENST00000588770.5:n.4089+35_4089+36delinsAT
NM_000227.4:c.4684+35_4684+36delinsAT NP_000218.3:n.4684+35_4684+36delinsAT
NM_001127717.2:c.9343+35_9343+36delinsAT NP_001121189.2:n.9343+35_9343+36delinsAT
NM_001127718.2:c.4516+35_4516+36delinsAT NP_001121190.2:n.4516+35_4516+36delinsAT
NM_198129.2:c.9511+35_9511+36delinsAT NP_937762.2:n.9511+35_9511+36delinsAT
XM_011525978.1:c.9538+35_9538+36delinsAT XP_011524280.1:n.9538+35_9538+36delinsAT
XM_011525979.1:c.9529+35_9529+36delinsAT XP_011524281.1:n.9529+35_9529+36delinsAT
XM_011525980.1:c.9520+35_9520+36delinsAT XP_011524282.1:n.9520+35_9520+36delinsAT
XM_011525981.1:c.9406+35_9406+36delinsAT XP_011524283.1:n.9406+35_9406+36delinsAT
XM_011525982.1:c.9241+35_9241+36delinsAT XP_011524284.1:n.9241+35_9241+36delinsAT
XM_011525978.2:c.9538+35_9538+36delinsAT XP_011524280.1:n.9538+35_9538+36delinsAT
XM_011525979.2:c.9529+35_9529+36delinsAT XP_011524281.1:n.9529+35_9529+36delinsAT
XM_011525980.2:c.9520+35_9520+36delinsAT XP_011524282.1:n.9520+35_9520+36delinsAT
XM_011525981.2:c.9406+35_9406+36delinsAT XP_011524283.1:n.9406+35_9406+36delinsAT
XM_011525982.2:c.9241+35_9241+36delinsAT XP_011524284.1:n.9241+35_9241+36delinsAT
XM_017025743.1:c.7390+35_7390+36delinsAT XP_016881232.1:n.7390+35_7390+36delinsAT
XM_017025744.1:c.5080+35_5080+36delinsAT XP_016881233.1:n.5080+35_5080+36delinsAT
XR_001753199.1:n.9779+35_9779+36delinsAT
NM_000227.5:c.4684+35_4684+36delinsAT NP_000218.3:n.4684+35_4684+36delinsAT
NM_001127717.3:c.9343+35_9343+36delinsAT NP_001121189.2:n.9343+35_9343+36delinsAT
NM_001127718.3:c.4516+35_4516+36delinsAT NP_001121190.2:n.4516+35_4516+36delinsAT
NM_198129.3:c.9511+35_9511+36delinsAT NP_937762.2:n.9511+35_9511+36delinsAT
NM_000227.6:c.4684+35_4684+36delinsAT MANE Plus Clinical NP_000218.3:n.4684+35_4684+36delinsAT
NM_001127717.4:c.9343+35_9343+36delinsAT NP_001121189.2:n.9343+35_9343+36delinsAT
NM_001127718.4:c.4516+35_4516+36delinsAT NP_001121190.2:n.4516+35_4516+36delinsAT
NM_198129.4:c.9511+35_9511+36delinsAT MANE Select NP_937762.2:n.9511+35_9511+36delinsAT