Canonical Allele Identifier: CA2680313517

Gene: LAMA2

Linked Data

• gnomAD v4: 6-129297962-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129297962_129297963insGG , CM000668.2:g.129297962_129297963insGG	GRCh38
NC_000006.11:g.129619107_129619108insGG , CM000668.1:g.129619107_129619108insGG	GRCh37
NC_000006.10:g.129660800_129660801insGG	NCBI36
NG_008678.1:g.419822_419823insGG , LRG_409:g.419822_419823insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.3037+97_3037+98insGG	ENSP00000481744.2:n.3037+97_3037+98insGG
ENST00000618192.5:c.3301+97_3301+98insGG	ENSP00000480802.2:n.3301+97_3301+98insGG
ENST00000421865.3:c.3037+97_3037+98insGG MANE Select	ENSP00000400365.2:n.3037+97_3037+98insGG
ENST00000421865.2:c.3037+97_3037+98insGG	ENSP00000400365.2:n.3037+97_3037+98insGG
ENST00000617695.4:c.3037+97_3037+98insGG	ENSP00000481744.1:n.3037+97_3037+98insGG
ENST00000618192.4:c.3037+97_3037+98insGG	ENSP00000480802.1:n.3037+97_3037+98insGG
NM_000426.3:c.3037+97_3037+98insGG , LRG_409t1:c.3037+97_3037+98insGG	NP_000417.2:n.3037+97_3037+98insGG
NM_001079823.1:c.3037+97_3037+98insGG	NP_001073291.1:n.3037+97_3037+98insGG
XM_005266981.2:c.3301+97_3301+98insGG	XP_005267038.1:n.3301+97_3301+98insGG
XM_005266982.2:c.3301+97_3301+98insGG	XP_005267039.1:n.3301+97_3301+98insGG
XM_011535820.1:c.3301+97_3301+98insGG	XP_011534122.1:n.3301+97_3301+98insGG
XM_005266981.3:c.3301+97_3301+98insGG	XP_005267038.1:n.3301+97_3301+98insGG
XM_005266982.3:c.3301+97_3301+98insGG	XP_005267039.1:n.3301+97_3301+98insGG
XM_011535820.2:c.3301+97_3301+98insGG	XP_011534122.1:n.3301+97_3301+98insGG
XM_017010851.2:c.3307+97_3307+98insGG	XP_016866340.1:n.3307+97_3307+98insGG
XM_017010852.1:c.1432+97_1432+98insGG	XP_016866341.1:n.1432+97_1432+98insGG
XM_017010853.1:c.3301+97_3301+98insGG	XP_016866342.1:n.3301+97_3301+98insGG
NM_000426.4:c.3037+97_3037+98insGG MANE Select	NP_000417.3:n.3037+97_3037+98insGG
NM_001079823.2:c.3037+97_3037+98insGG	NP_001073291.2:n.3037+97_3037+98insGG