Canonical Allele Identifier: CA2576473122

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915368_23915369insAA , CM000680.2:g.23915368_23915369insAA	GRCh38
NC_000018.9:g.21495332_21495333insAA , CM000680.1:g.21495332_21495333insAA	GRCh37
NC_000018.8:g.19749330_19749331insAA	NCBI36
NG_007853.2:g.230771_230772insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2897_2898insAA MANE Plus Clinical	ENSP00000269217.5:p.Tyr966Ter
ENST00000313654.14:c.7724_7725insAA MANE Select	ENSP00000324532.8:p.Tyr2575Ter
ENST00000649721.1:c.4319_4320insAA	ENSP00000497885.1:p.Tyr1440Ter
ENST00000269217.10:c.2897_2898insAA	ENSP00000269217.5:p.Tyr966Ter
ENST00000313654.13:c.7724_7725insAA	ENSP00000324532.8:p.Tyr2575Ter
ENST00000399516.7:c.7556_7557insAA	ENSP00000382432.2:p.Tyr2519Ter
ENST00000586751.5:c.2502_2503insAA
ENST00000587184.5:c.2729_2730insAA	ENSP00000466557.1:p.Tyr910Ter
ENST00000588770.5:n.2302_2303insAA
NM_000227.4:c.2897_2898insAA	NP_000218.3:p.Tyr966Ter
NM_001127717.2:c.7556_7557insAA	NP_001121189.2:p.Tyr2519Ter
NM_001127718.2:c.2729_2730insAA	NP_001121190.2:p.Tyr910Ter
NM_198129.2:c.7724_7725insAA	NP_937762.2:p.Tyr2575Ter
XM_011525978.1:c.7751_7752insAA	XP_011524280.1:p.Tyr2584Ter
XM_011525979.1:c.7742_7743insAA	XP_011524281.1:p.Tyr2581Ter
XM_011525980.1:c.7733_7734insAA	XP_011524282.1:p.Tyr2578Ter
XM_011525981.1:c.7619_7620insAA	XP_011524283.1:p.Tyr2540Ter
XM_011525982.1:c.7454_7455insAA	XP_011524284.1:p.Tyr2485Ter
XM_011525978.2:c.7751_7752insAA	XP_011524280.1:p.Tyr2584Ter
XM_011525979.2:c.7742_7743insAA	XP_011524281.1:p.Tyr2581Ter
XM_011525980.2:c.7733_7734insAA	XP_011524282.1:p.Tyr2578Ter
XM_011525981.2:c.7619_7620insAA	XP_011524283.1:p.Tyr2540Ter
XM_011525982.2:c.7454_7455insAA	XP_011524284.1:p.Tyr2485Ter
XM_017025743.1:c.5603_5604insAA	XP_016881232.1:p.Tyr1868Ter
XM_017025744.1:c.3293_3294insAA	XP_016881233.1:p.Tyr1098Ter
XR_001753199.1:n.7992_7993insAA
NM_000227.5:c.2897_2898insAA	NP_000218.3:p.Tyr966Ter
NM_001127717.3:c.7556_7557insAA	NP_001121189.2:p.Tyr2519Ter
NM_001127718.3:c.2729_2730insAA	NP_001121190.2:p.Tyr910Ter
NM_198129.3:c.7724_7725insAA	NP_937762.2:p.Tyr2575Ter
NM_000227.6:c.2897_2898insAA MANE Plus Clinical	NP_000218.3:p.Tyr966Ter
NM_001127717.4:c.7556_7557insAA	NP_001121189.2:p.Tyr2519Ter
NM_001127718.4:c.2729_2730insAA	NP_001121190.2:p.Tyr910Ter
NM_198129.4:c.7724_7725insAA MANE Select	NP_937762.2:p.Tyr2575Ter