Canonical Allele Identifier: CA2641297067

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23915360-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915361del , CM000680.2:g.23915361del	GRCh38
NC_000018.9:g.21495325del , CM000680.1:g.21495325del	GRCh37
NC_000018.8:g.19749323del	NCBI36
NG_007853.2:g.230764del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2890del MANE Plus Clinical	ENSP00000269217.5:p.Ser964AlafsTer?
ENST00000313654.14:c.7717del MANE Select	ENSP00000324532.8:p.Ser2573AlafsTer?
ENST00000649721.1:c.4312del	ENSP00000497885.1:p.Ser1438AlafsTer?
ENST00000269217.10:c.2890del	ENSP00000269217.5:p.Ser964AlafsTer?
ENST00000313654.13:c.7717del	ENSP00000324532.8:p.Ser2573AlafsTer?
ENST00000399516.7:c.7549del	ENSP00000382432.2:p.Ser2517AlafsTer?
ENST00000586751.5:c.2495del
ENST00000587184.5:c.2722del	ENSP00000466557.1:p.Ser908AlafsTer?
ENST00000588770.5:n.2295del
NM_000227.4:c.2890del	NP_000218.3:p.Ser964AlafsTer?
NM_001127717.2:c.7549del	NP_001121189.2:p.Ser2517AlafsTer?
NM_001127718.2:c.2722del	NP_001121190.2:p.Ser908AlafsTer?
NM_198129.2:c.7717del	NP_937762.2:p.Ser2573AlafsTer?
XM_011525978.1:c.7744del	XP_011524280.1:p.Ser2582AlafsTer?
XM_011525979.1:c.7735del	XP_011524281.1:p.Ser2579AlafsTer?
XM_011525980.1:c.7726del	XP_011524282.1:p.Ser2576AlafsTer?
XM_011525981.1:c.7612del	XP_011524283.1:p.Ser2538AlafsTer?
XM_011525982.1:c.7447del	XP_011524284.1:p.Ser2483AlafsTer?
XM_011525978.2:c.7744del	XP_011524280.1:p.Ser2582AlafsTer?
XM_011525979.2:c.7735del	XP_011524281.1:p.Ser2579AlafsTer?
XM_011525980.2:c.7726del	XP_011524282.1:p.Ser2576AlafsTer?
XM_011525981.2:c.7612del	XP_011524283.1:p.Ser2538AlafsTer?
XM_011525982.2:c.7447del	XP_011524284.1:p.Ser2483AlafsTer?
XM_017025743.1:c.5596del	XP_016881232.1:p.Ser1866AlafsTer?
XM_017025744.1:c.3286del	XP_016881233.1:p.Ser1096AlafsTer?
XR_001753199.1:n.7985del
NM_000227.5:c.2890del	NP_000218.3:p.Ser964AlafsTer?
NM_001127717.3:c.7549del	NP_001121189.2:p.Ser2517AlafsTer?
NM_001127718.3:c.2722del	NP_001121190.2:p.Ser908AlafsTer?
NM_198129.3:c.7717del	NP_937762.2:p.Ser2573AlafsTer?
NM_000227.6:c.2890del MANE Plus Clinical	NP_000218.3:p.Ser964AlafsTer?
NM_001127717.4:c.7549del	NP_001121189.2:p.Ser2517AlafsTer?
NM_001127718.4:c.2722del	NP_001121190.2:p.Ser908AlafsTer?
NM_198129.4:c.7717del MANE Select	NP_937762.2:p.Ser2573AlafsTer?