Canonical Allele Identifier: CA2576553376

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898852del , CM000680.2:g.23898852del	GRCh38
NC_000018.9:g.21478816del , CM000680.1:g.21478816del	GRCh37
NC_000018.8:g.19732814del	NCBI36
NG_007853.2:g.214255del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.897+4del MANE Plus Clinical	ENSP00000269217.5:n.897+4del
ENST00000313654.14:c.5724+4del MANE Select	ENSP00000324532.8:n.5724+4del
ENST00000649721.1:c.2616+4del	ENSP00000497885.1:n.2616+4del
ENST00000269217.10:c.897+4del	ENSP00000269217.5:n.897+4del
ENST00000313654.13:c.5724+4del	ENSP00000324532.8:n.5724+4del
ENST00000399516.7:c.5724+4del	ENSP00000382432.2:n.5724+4del
ENST00000586709.1:n.112+4del
ENST00000586751.5:c.502+4del
ENST00000587184.5:c.897+4del	ENSP00000466557.1:n.897+4del
ENST00000588770.5:n.302+4del
NM_000227.4:c.897+4del	NP_000218.3:n.897+4del
NM_001127717.2:c.5724+4del	NP_001121189.2:n.5724+4del
NM_001127718.2:c.897+4del	NP_001121190.2:n.897+4del
NM_198129.2:c.5724+4del	NP_937762.2:n.5724+4del
XM_011525978.1:c.5751+4del	XP_011524280.1:n.5751+4del
XM_011525979.1:c.5742+4del	XP_011524281.1:n.5742+4del
XM_011525980.1:c.5733+4del	XP_011524282.1:n.5733+4del
XM_011525981.1:c.5619+4del	XP_011524283.1:n.5619+4del
XM_011525982.1:c.5751+4del	XP_011524284.1:n.5751+4del
XM_011525978.2:c.5751+4del	XP_011524280.1:n.5751+4del
XM_011525979.2:c.5742+4del	XP_011524281.1:n.5742+4del
XM_011525980.2:c.5733+4del	XP_011524282.1:n.5733+4del
XM_011525981.2:c.5619+4del	XP_011524283.1:n.5619+4del
XM_011525982.2:c.5751+4del	XP_011524284.1:n.5751+4del
XM_017025743.1:c.3603+4del	XP_016881232.1:n.3603+4del
XM_017025744.1:c.1293+4del	XP_016881233.1:n.1293+4del
XR_001753199.1:n.5992+4del
NM_000227.5:c.897+4del	NP_000218.3:n.897+4del
NM_001127717.3:c.5724+4del	NP_001121189.2:n.5724+4del
NM_001127718.3:c.897+4del	NP_001121190.2:n.897+4del
NM_198129.3:c.5724+4del	NP_937762.2:n.5724+4del
NM_000227.6:c.897+4del MANE Plus Clinical	NP_000218.3:n.897+4del
NM_001127717.4:c.5724+4del	NP_001121189.2:n.5724+4del
NM_001127718.4:c.897+4del	NP_001121190.2:n.897+4del
NM_198129.4:c.5724+4del MANE Select	NP_937762.2:n.5724+4del