Canonical Allele Identifier: CA2290312315

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876285_23876286delinsGA , CM000680.2:g.23876285_23876286delinsGA	GRCh38
NC_000018.9:g.21456249_21456250delinsGA , CM000680.1:g.21456249_21456250delinsGA	GRCh37
NC_000018.8:g.19710247_19710248delinsGA	NCBI36
NG_007853.2:g.191688_191689delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.172-9_172-8delinsGA MANE Plus Clinical	ENSP00000269217.5:n.172-9_172-8delinsGA
ENST00000313654.14:c.4999-9_4999-8delinsGA MANE Select	ENSP00000324532.8:n.4999-9_4999-8delinsGA
ENST00000649721.1:c.1891-9_1891-8delinsGA	ENSP00000497885.1:n.1891-9_1891-8delinsGA
ENST00000269217.10:c.172-9_172-8delinsGA	ENSP00000269217.5:n.172-9_172-8delinsGA
ENST00000313654.13:c.4999-9_4999-8delinsGA	ENSP00000324532.8:n.4999-9_4999-8delinsGA
ENST00000399516.7:c.4999-9_4999-8delinsGA	ENSP00000382432.2:n.4999-9_4999-8delinsGA
ENST00000587184.5:c.172-9_172-8delinsGA	ENSP00000466557.1:n.172-9_172-8delinsGA
NM_000227.4:c.172-9_172-8delinsGA	NP_000218.3:n.172-9_172-8delinsGA
NM_001127717.2:c.4999-9_4999-8delinsGA	NP_001121189.2:n.4999-9_4999-8delinsGA
NM_001127718.2:c.172-9_172-8delinsGA	NP_001121190.2:n.172-9_172-8delinsGA
NM_198129.2:c.4999-9_4999-8delinsGA	NP_937762.2:n.4999-9_4999-8delinsGA
XM_011525978.1:c.5026-9_5026-8delinsGA	XP_011524280.1:n.5026-9_5026-8delinsGA
XM_011525979.1:c.5017-9_5017-8delinsGA	XP_011524281.1:n.5017-9_5017-8delinsGA
XM_011525980.1:c.5008-9_5008-8delinsGA	XP_011524282.1:n.5008-9_5008-8delinsGA
XM_011525981.1:c.4894-9_4894-8delinsGA	XP_011524283.1:n.4894-9_4894-8delinsGA
XM_011525982.1:c.5026-9_5026-8delinsGA	XP_011524284.1:n.5026-9_5026-8delinsGA
XM_011525978.2:c.5026-9_5026-8delinsGA	XP_011524280.1:n.5026-9_5026-8delinsGA
XM_011525979.2:c.5017-9_5017-8delinsGA	XP_011524281.1:n.5017-9_5017-8delinsGA
XM_011525980.2:c.5008-9_5008-8delinsGA	XP_011524282.1:n.5008-9_5008-8delinsGA
XM_011525981.2:c.4894-9_4894-8delinsGA	XP_011524283.1:n.4894-9_4894-8delinsGA
XM_011525982.2:c.5026-9_5026-8delinsGA	XP_011524284.1:n.5026-9_5026-8delinsGA
XM_017025743.1:c.2878-9_2878-8delinsGA	XP_016881232.1:n.2878-9_2878-8delinsGA
XM_017025744.1:c.568-9_568-8delinsGA	XP_016881233.1:n.568-9_568-8delinsGA
XR_001753199.1:n.5267-9_5267-8delinsGA
NM_000227.5:c.172-9_172-8delinsGA	NP_000218.3:n.172-9_172-8delinsGA
NM_001127717.3:c.4999-9_4999-8delinsGA	NP_001121189.2:n.4999-9_4999-8delinsGA
NM_001127718.3:c.172-9_172-8delinsGA	NP_001121190.2:n.172-9_172-8delinsGA
NM_198129.3:c.4999-9_4999-8delinsGA	NP_937762.2:n.4999-9_4999-8delinsGA
NM_000227.6:c.172-9_172-8delinsGA MANE Plus Clinical	NP_000218.3:n.172-9_172-8delinsGA
NM_001127717.4:c.4999-9_4999-8delinsGA	NP_001121189.2:n.4999-9_4999-8delinsGA
NM_001127718.4:c.172-9_172-8delinsGA	NP_001121190.2:n.172-9_172-8delinsGA
NM_198129.4:c.4999-9_4999-8delinsGA MANE Select	NP_937762.2:n.4999-9_4999-8delinsGA