Canonical Allele Identifier: CA2641299253

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23949963-TAAGAACTGTATCCTGTTTTCTTTCATGGTGATGCTTTAACTTTTGCTTTGTTTCTCTTTTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23949967_23950028del , CM000680.2:g.23949967_23950028del	GRCh38
NC_000018.9:g.21529931_21529992del , CM000680.1:g.21529931_21529992del	GRCh37
NC_000018.8:g.19783929_19783990del	NCBI36
NG_007853.2:g.265370_265431del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4684+43_4685-1del MANE Plus Clinical	ENSP00000269217.5:n.4684+43_4685-1del
ENST00000313654.14:c.9511+43_9512-1del MANE Select	ENSP00000324532.8:n.9511+43_9512-1del
ENST00000649721.1:c.6106+43_6107-1del	ENSP00000497885.1:n.6106+43_6107-1del
ENST00000269217.10:c.4684+43_4685-1del	ENSP00000269217.5:n.4684+43_4685-1del
ENST00000313654.13:c.9511+43_9512-1del	ENSP00000324532.8:n.9511+43_9512-1del
ENST00000399516.7:c.9343+43_9344-1del	ENSP00000382432.2:n.9343+43_9344-1del
ENST00000587184.5:c.4516+43_4517-1del	ENSP00000466557.1:n.4516+43_4517-1del
ENST00000588004.1:c.32+43_33-1del
ENST00000588770.5:n.4089+43_4090-1del
NM_000227.4:c.4684+43_4685-1del	NP_000218.3:n.4684+43_4685-1del
NM_001127717.2:c.9343+43_9344-1del	NP_001121189.2:n.9343+43_9344-1del
NM_001127718.2:c.4516+43_4517-1del	NP_001121190.2:n.4516+43_4517-1del
NM_198129.2:c.9511+43_9512-1del	NP_937762.2:n.9511+43_9512-1del
XM_011525978.1:c.9538+43_9539-1del	XP_011524280.1:n.9538+43_9539-1del
XM_011525979.1:c.9529+43_9530-1del	XP_011524281.1:n.9529+43_9530-1del
XM_011525980.1:c.9520+43_9521-1del	XP_011524282.1:n.9520+43_9521-1del
XM_011525981.1:c.9406+43_9407-1del	XP_011524283.1:n.9406+43_9407-1del
XM_011525982.1:c.9241+43_9242-1del	XP_011524284.1:n.9241+43_9242-1del
XM_011525978.2:c.9538+43_9539-1del	XP_011524280.1:n.9538+43_9539-1del
XM_011525979.2:c.9529+43_9530-1del	XP_011524281.1:n.9529+43_9530-1del
XM_011525980.2:c.9520+43_9521-1del	XP_011524282.1:n.9520+43_9521-1del
XM_011525981.2:c.9406+43_9407-1del	XP_011524283.1:n.9406+43_9407-1del
XM_011525982.2:c.9241+43_9242-1del	XP_011524284.1:n.9241+43_9242-1del
XM_017025743.1:c.7390+43_7391-1del	XP_016881232.1:n.7390+43_7391-1del
XM_017025744.1:c.5080+43_5081-1del	XP_016881233.1:n.5080+43_5081-1del
XR_001753199.1:n.9779+43_9780-1del
NM_000227.5:c.4684+43_4685-1del	NP_000218.3:n.4684+43_4685-1del
NM_001127717.3:c.9343+43_9344-1del	NP_001121189.2:n.9343+43_9344-1del
NM_001127718.3:c.4516+43_4517-1del	NP_001121190.2:n.4516+43_4517-1del
NM_198129.3:c.9511+43_9512-1del	NP_937762.2:n.9511+43_9512-1del
NM_000227.6:c.4684+43_4685-1del MANE Plus Clinical	NP_000218.3:n.4684+43_4685-1del
NM_001127717.4:c.9343+43_9344-1del	NP_001121189.2:n.9343+43_9344-1del
NM_001127718.4:c.4516+43_4517-1del	NP_001121190.2:n.4516+43_4517-1del
NM_198129.4:c.9511+43_9512-1del MANE Select	NP_937762.2:n.9511+43_9512-1del