Canonical Allele Identifier: CA2290343968

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23949974_23949975delinsTC , CM000680.2:g.23949974_23949975delinsTC	GRCh38
NC_000018.9:g.21529938_21529939delinsTC , CM000680.1:g.21529938_21529939delinsTC	GRCh37
NC_000018.8:g.19783936_19783937delinsTC	NCBI36
NG_007853.2:g.265377_265378delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4684+50_4684+51delinsTC MANE Plus Clinical	ENSP00000269217.5:n.4684+50_4684+51delinsTC
ENST00000313654.14:c.9511+50_9511+51delinsTC MANE Select	ENSP00000324532.8:n.9511+50_9511+51delinsTC
ENST00000649721.1:c.6106+50_6106+51delinsTC	ENSP00000497885.1:n.6106+50_6106+51delinsTC
ENST00000269217.10:c.4684+50_4684+51delinsTC	ENSP00000269217.5:n.4684+50_4684+51delinsTC
ENST00000313654.13:c.9511+50_9511+51delinsTC	ENSP00000324532.8:n.9511+50_9511+51delinsTC
ENST00000399516.7:c.9343+50_9343+51delinsTC	ENSP00000382432.2:n.9343+50_9343+51delinsTC
ENST00000587184.5:c.4516+50_4516+51delinsTC	ENSP00000466557.1:n.4516+50_4516+51delinsTC
ENST00000588004.1:c.32+50_32+51delinsTC
ENST00000588770.5:n.4089+50_4089+51delinsTC
NM_000227.4:c.4684+50_4684+51delinsTC	NP_000218.3:n.4684+50_4684+51delinsTC
NM_001127717.2:c.9343+50_9343+51delinsTC	NP_001121189.2:n.9343+50_9343+51delinsTC
NM_001127718.2:c.4516+50_4516+51delinsTC	NP_001121190.2:n.4516+50_4516+51delinsTC
NM_198129.2:c.9511+50_9511+51delinsTC	NP_937762.2:n.9511+50_9511+51delinsTC
XM_011525978.1:c.9538+50_9538+51delinsTC	XP_011524280.1:n.9538+50_9538+51delinsTC
XM_011525979.1:c.9529+50_9529+51delinsTC	XP_011524281.1:n.9529+50_9529+51delinsTC
XM_011525980.1:c.9520+50_9520+51delinsTC	XP_011524282.1:n.9520+50_9520+51delinsTC
XM_011525981.1:c.9406+50_9406+51delinsTC	XP_011524283.1:n.9406+50_9406+51delinsTC
XM_011525982.1:c.9241+50_9241+51delinsTC	XP_011524284.1:n.9241+50_9241+51delinsTC
XM_011525978.2:c.9538+50_9538+51delinsTC	XP_011524280.1:n.9538+50_9538+51delinsTC
XM_011525979.2:c.9529+50_9529+51delinsTC	XP_011524281.1:n.9529+50_9529+51delinsTC
XM_011525980.2:c.9520+50_9520+51delinsTC	XP_011524282.1:n.9520+50_9520+51delinsTC
XM_011525981.2:c.9406+50_9406+51delinsTC	XP_011524283.1:n.9406+50_9406+51delinsTC
XM_011525982.2:c.9241+50_9241+51delinsTC	XP_011524284.1:n.9241+50_9241+51delinsTC
XM_017025743.1:c.7390+50_7390+51delinsTC	XP_016881232.1:n.7390+50_7390+51delinsTC
XM_017025744.1:c.5080+50_5080+51delinsTC	XP_016881233.1:n.5080+50_5080+51delinsTC
XR_001753199.1:n.9779+50_9779+51delinsTC
NM_000227.5:c.4684+50_4684+51delinsTC	NP_000218.3:n.4684+50_4684+51delinsTC
NM_001127717.3:c.9343+50_9343+51delinsTC	NP_001121189.2:n.9343+50_9343+51delinsTC
NM_001127718.3:c.4516+50_4516+51delinsTC	NP_001121190.2:n.4516+50_4516+51delinsTC
NM_198129.3:c.9511+50_9511+51delinsTC	NP_937762.2:n.9511+50_9511+51delinsTC
NM_000227.6:c.4684+50_4684+51delinsTC MANE Plus Clinical	NP_000218.3:n.4684+50_4684+51delinsTC
NM_001127717.4:c.9343+50_9343+51delinsTC	NP_001121189.2:n.9343+50_9343+51delinsTC
NM_001127718.4:c.4516+50_4516+51delinsTC	NP_001121190.2:n.4516+50_4516+51delinsTC
NM_198129.4:c.9511+50_9511+51delinsTC MANE Select	NP_937762.2:n.9511+50_9511+51delinsTC