Canonical Allele Identifier: CA1094379190

Gene: LAMA2

Linked Data

• dbSNP Id: rs775185063
• gnomAD v4: 6-129250320-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129250328_129250329dup , CM000668.2:g.129250328_129250329dup	GRCh38
NC_000006.11:g.129571473_129571474dup , CM000668.1:g.129571473_129571474dup	GRCh37
NC_000006.10:g.129613166_129613167dup	NCBI36
NG_008678.1:g.372188_372189dup , LRG_409:g.372188_372189dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.1884+115_1884+116dup	ENSP00000481744.2:n.1884+115_1884+116dup
ENST00000618192.5:c.1884+115_1884+116dup	ENSP00000480802.2:n.1884+115_1884+116dup
ENST00000421865.3:c.1884+115_1884+116dup MANE Select	ENSP00000400365.2:n.1884+115_1884+116dup
ENST00000421865.2:c.1884+115_1884+116dup	ENSP00000400365.2:n.1884+115_1884+116dup
ENST00000617695.4:c.1884+115_1884+116dup	ENSP00000481744.1:n.1884+115_1884+116dup
ENST00000618192.4:c.1884+115_1884+116dup	ENSP00000480802.1:n.1884+115_1884+116dup
NM_000426.3:c.1884+115_1884+116dup , LRG_409t1:c.1884+115_1884+116dup	NP_000417.2:n.1884+115_1884+116dup
NM_001079823.1:c.1884+115_1884+116dup	NP_001073291.1:n.1884+115_1884+116dup
XM_005266981.2:c.1884+115_1884+116dup	XP_005267038.1:n.1884+115_1884+116dup
XM_005266982.2:c.1884+115_1884+116dup	XP_005267039.1:n.1884+115_1884+116dup
XM_011535820.1:c.1884+115_1884+116dup	XP_011534122.1:n.1884+115_1884+116dup
XM_005266981.3:c.1884+115_1884+116dup	XP_005267038.1:n.1884+115_1884+116dup
XM_005266982.3:c.1884+115_1884+116dup	XP_005267039.1:n.1884+115_1884+116dup
XM_011535820.2:c.1884+115_1884+116dup	XP_011534122.1:n.1884+115_1884+116dup
XM_017010851.2:c.1890+115_1890+116dup	XP_016866340.1:n.1890+115_1890+116dup
XM_017010852.1:c.15+115_15+116dup	XP_016866341.1:n.15+115_15+116dup
XM_017010853.1:c.1884+115_1884+116dup	XP_016866342.1:n.1884+115_1884+116dup
NM_000426.4:c.1884+115_1884+116dup MANE Select	NP_000417.3:n.1884+115_1884+116dup
NM_001079823.2:c.1884+115_1884+116dup	NP_001073291.2:n.1884+115_1884+116dup