Canonical Allele Identifier: CA1663102781

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129297898_129297900delinsACT , CM000668.2:g.129297898_129297900delinsACT	GRCh38
NC_000006.11:g.129619043_129619045delinsACT , CM000668.1:g.129619043_129619045delinsACT	GRCh37
NC_000006.10:g.129660736_129660738delinsACT	NCBI36
NG_008678.1:g.419758_419760delinsACT , LRG_409:g.419758_419760delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.3037+33_3037+35delinsACT	ENSP00000481744.2:n.3037+33_3037+35delinsACT
ENST00000618192.5:c.3301+33_3301+35delinsACT	ENSP00000480802.2:n.3301+33_3301+35delinsACT
ENST00000421865.3:c.3037+33_3037+35delinsACT MANE Select	ENSP00000400365.2:n.3037+33_3037+35delinsACT
ENST00000421865.2:c.3037+33_3037+35delinsACT	ENSP00000400365.2:n.3037+33_3037+35delinsACT
ENST00000617695.4:c.3037+33_3037+35delinsACT	ENSP00000481744.1:n.3037+33_3037+35delinsACT
ENST00000618192.4:c.3037+33_3037+35delinsACT	ENSP00000480802.1:n.3037+33_3037+35delinsACT
NM_000426.3:c.3037+33_3037+35delinsACT , LRG_409t1:c.3037+33_3037+35delinsACT	NP_000417.2:n.3037+33_3037+35delinsACT
NM_001079823.1:c.3037+33_3037+35delinsACT	NP_001073291.1:n.3037+33_3037+35delinsACT
XM_005266981.2:c.3301+33_3301+35delinsACT	XP_005267038.1:n.3301+33_3301+35delinsACT
XM_005266982.2:c.3301+33_3301+35delinsACT	XP_005267039.1:n.3301+33_3301+35delinsACT
XM_011535820.1:c.3301+33_3301+35delinsACT	XP_011534122.1:n.3301+33_3301+35delinsACT
XM_005266981.3:c.3301+33_3301+35delinsACT	XP_005267038.1:n.3301+33_3301+35delinsACT
XM_005266982.3:c.3301+33_3301+35delinsACT	XP_005267039.1:n.3301+33_3301+35delinsACT
XM_011535820.2:c.3301+33_3301+35delinsACT	XP_011534122.1:n.3301+33_3301+35delinsACT
XM_017010851.2:c.3307+33_3307+35delinsACT	XP_016866340.1:n.3307+33_3307+35delinsACT
XM_017010852.1:c.1432+33_1432+35delinsACT	XP_016866341.1:n.1432+33_1432+35delinsACT
XM_017010853.1:c.3301+33_3301+35delinsACT	XP_016866342.1:n.3301+33_3301+35delinsACT
NM_000426.4:c.3037+33_3037+35delinsACT MANE Select	NP_000417.3:n.3037+33_3037+35delinsACT
NM_001079823.2:c.3037+33_3037+35delinsACT	NP_001073291.2:n.3037+33_3037+35delinsACT