Canonical Allele Identifier: CA2541308490

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23904426_23904427insAAGTGGA , CM000680.2:g.23904426_23904427insAAGTGGA	GRCh38
NC_000018.9:g.21484390_21484391insAAGTGGA , CM000680.1:g.21484390_21484391insAAGTGGA	GRCh37
NC_000018.8:g.19738388_19738389insAAGTGGA	NCBI36
NG_007853.2:g.219829_219830insAAGTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1647-127_1647-126insAAGTGGA MANE Plus Clinical	ENSP00000269217.5:n.1647-127_1647-126insAAGTGGA
ENST00000313654.14:c.6474-127_6474-126insAAGTGGA MANE Select	ENSP00000324532.8:n.6474-127_6474-126insAAGTGGA
ENST00000649721.1:c.3366-127_3366-126insAAGTGGA	ENSP00000497885.1:n.3366-127_3366-126insAAGTGGA
ENST00000269217.10:c.1647-127_1647-126insAAGTGGA	ENSP00000269217.5:n.1647-127_1647-126insAAGTGGA
ENST00000313654.13:c.6474-127_6474-126insAAGTGGA	ENSP00000324532.8:n.6474-127_6474-126insAAGTGGA
ENST00000399516.7:c.6306-127_6306-126insAAGTGGA	ENSP00000382432.2:n.6306-127_6306-126insAAGTGGA
ENST00000586751.5:c.1252-127_1252-126insAAGTGGA
ENST00000587184.5:c.1479-127_1479-126insAAGTGGA	ENSP00000466557.1:n.1479-127_1479-126insAAGTGGA
ENST00000588770.5:n.1052-127_1052-126insAAGTGGA
NM_000227.4:c.1647-127_1647-126insAAGTGGA	NP_000218.3:n.1647-127_1647-126insAAGTGGA
NM_001127717.2:c.6306-127_6306-126insAAGTGGA	NP_001121189.2:n.6306-127_6306-126insAAGTGGA
NM_001127718.2:c.1479-127_1479-126insAAGTGGA	NP_001121190.2:n.1479-127_1479-126insAAGTGGA
NM_198129.2:c.6474-127_6474-126insAAGTGGA	NP_937762.2:n.6474-127_6474-126insAAGTGGA
XM_011525978.1:c.6501-127_6501-126insAAGTGGA	XP_011524280.1:n.6501-127_6501-126insAAGTGGA
XM_011525979.1:c.6492-127_6492-126insAAGTGGA	XP_011524281.1:n.6492-127_6492-126insAAGTGGA
XM_011525980.1:c.6483-127_6483-126insAAGTGGA	XP_011524282.1:n.6483-127_6483-126insAAGTGGA
XM_011525981.1:c.6369-127_6369-126insAAGTGGA	XP_011524283.1:n.6369-127_6369-126insAAGTGGA
XM_011525982.1:c.6501-127_6501-126insAAGTGGA	XP_011524284.1:n.6501-127_6501-126insAAGTGGA
XM_011525978.2:c.6501-127_6501-126insAAGTGGA	XP_011524280.1:n.6501-127_6501-126insAAGTGGA
XM_011525979.2:c.6492-127_6492-126insAAGTGGA	XP_011524281.1:n.6492-127_6492-126insAAGTGGA
XM_011525980.2:c.6483-127_6483-126insAAGTGGA	XP_011524282.1:n.6483-127_6483-126insAAGTGGA
XM_011525981.2:c.6369-127_6369-126insAAGTGGA	XP_011524283.1:n.6369-127_6369-126insAAGTGGA
XM_011525982.2:c.6501-127_6501-126insAAGTGGA	XP_011524284.1:n.6501-127_6501-126insAAGTGGA
XM_017025743.1:c.4353-127_4353-126insAAGTGGA	XP_016881232.1:n.4353-127_4353-126insAAGTGGA
XM_017025744.1:c.2043-127_2043-126insAAGTGGA	XP_016881233.1:n.2043-127_2043-126insAAGTGGA
XR_001753199.1:n.6742-127_6742-126insAAGTGGA
NM_000227.5:c.1647-127_1647-126insAAGTGGA	NP_000218.3:n.1647-127_1647-126insAAGTGGA
NM_001127717.3:c.6306-127_6306-126insAAGTGGA	NP_001121189.2:n.6306-127_6306-126insAAGTGGA
NM_001127718.3:c.1479-127_1479-126insAAGTGGA	NP_001121190.2:n.1479-127_1479-126insAAGTGGA
NM_198129.3:c.6474-127_6474-126insAAGTGGA	NP_937762.2:n.6474-127_6474-126insAAGTGGA
NM_000227.6:c.1647-127_1647-126insAAGTGGA MANE Plus Clinical	NP_000218.3:n.1647-127_1647-126insAAGTGGA
NM_001127717.4:c.6306-127_6306-126insAAGTGGA	NP_001121189.2:n.6306-127_6306-126insAAGTGGA
NM_001127718.4:c.1479-127_1479-126insAAGTGGA	NP_001121190.2:n.1479-127_1479-126insAAGTGGA
NM_198129.4:c.6474-127_6474-126insAAGTGGA MANE Select	NP_937762.2:n.6474-127_6474-126insAAGTGGA