Canonical Allele Identifier: CA2641299260

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23949988-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23949989del , CM000680.2:g.23949989del	GRCh38
NC_000018.9:g.21529953del , CM000680.1:g.21529953del	GRCh37
NC_000018.8:g.19783951del	NCBI36
NG_007853.2:g.265392del

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.4685-40del MANE Plus Clinical	ENSP00000269217.5:n.4685-40del
ENST00000313654.14:c.9512-40del MANE Select	ENSP00000324532.8:n.9512-40del
ENST00000649721.1:c.6107-40del	ENSP00000497885.1:n.6107-40del
ENST00000269217.10:c.4685-40del	ENSP00000269217.5:n.4685-40del
ENST00000313654.13:c.9512-40del	ENSP00000324532.8:n.9512-40del
ENST00000399516.7:c.9344-40del	ENSP00000382432.2:n.9344-40del
ENST00000587184.5:c.4517-40del	ENSP00000466557.1:n.4517-40del
ENST00000588004.1:c.33-40del
ENST00000588770.5:n.4090-40del
NM_000227.4:c.4685-40del	NP_000218.3:n.4685-40del
NM_001127717.2:c.9344-40del	NP_001121189.2:n.9344-40del
NM_001127718.2:c.4517-40del	NP_001121190.2:n.4517-40del
NM_198129.2:c.9512-40del	NP_937762.2:n.9512-40del
XM_011525978.1:c.9539-40del	XP_011524280.1:n.9539-40del
XM_011525979.1:c.9530-40del	XP_011524281.1:n.9530-40del
XM_011525980.1:c.9521-40del	XP_011524282.1:n.9521-40del
XM_011525981.1:c.9407-40del	XP_011524283.1:n.9407-40del
XM_011525982.1:c.9242-40del	XP_011524284.1:n.9242-40del
XM_011525978.2:c.9539-40del	XP_011524280.1:n.9539-40del
XM_011525979.2:c.9530-40del	XP_011524281.1:n.9530-40del
XM_011525980.2:c.9521-40del	XP_011524282.1:n.9521-40del
XM_011525981.2:c.9407-40del	XP_011524283.1:n.9407-40del
XM_011525982.2:c.9242-40del	XP_011524284.1:n.9242-40del
XM_017025743.1:c.7391-40del	XP_016881232.1:n.7391-40del
XM_017025744.1:c.5081-40del	XP_016881233.1:n.5081-40del
XR_001753199.1:n.9780-40del
NM_000227.5:c.4685-40del	NP_000218.3:n.4685-40del
NM_001127717.3:c.9344-40del	NP_001121189.2:n.9344-40del
NM_001127718.3:c.4517-40del	NP_001121190.2:n.4517-40del
NM_198129.3:c.9512-40del	NP_937762.2:n.9512-40del
NM_000227.6:c.4685-40del MANE Plus Clinical	NP_000218.3:n.4685-40del
NM_001127717.4:c.9344-40del	NP_001121189.2:n.9344-40del
NM_001127718.4:c.4517-40del	NP_001121190.2:n.4517-40del
NM_198129.4:c.9512-40del MANE Select	NP_937762.2:n.9512-40del