Canonical Allele Identifier: CA1663045476

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129190369_129190370delinsGT , CM000668.2:g.129190369_129190370delinsGT	GRCh38
NC_000006.11:g.129511514_129511515delinsGT , CM000668.1:g.129511514_129511515delinsGT	GRCh37
NC_000006.10:g.129553207_129553208delinsGT	NCBI36
NG_008678.1:g.312229_312230delinsGT , LRG_409:g.312229_312230delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.1608+24_1608+25delinsGT	ENSP00000481744.2:n.1608+24_1608+25delinsGT
ENST00000618192.5:c.1608+24_1608+25delinsGT	ENSP00000480802.2:n.1608+24_1608+25delinsGT
ENST00000686599.1:n.1713+24_1713+25delinsGT
ENST00000690881.1:n.1071+24_1071+25delinsGT
ENST00000421865.3:c.1608+24_1608+25delinsGT MANE Select	ENSP00000400365.2:n.1608+24_1608+25delinsGT
ENST00000421865.2:c.1608+24_1608+25delinsGT	ENSP00000400365.2:n.1608+24_1608+25delinsGT
ENST00000617695.4:c.1608+24_1608+25delinsGT	ENSP00000481744.1:n.1608+24_1608+25delinsGT
ENST00000618192.4:c.1608+24_1608+25delinsGT	ENSP00000480802.1:n.1608+24_1608+25delinsGT
NM_000426.3:c.1608+24_1608+25delinsGT , LRG_409t1:c.1608+24_1608+25delinsGT	NP_000417.2:n.1608+24_1608+25delinsGT
NM_001079823.1:c.1608+24_1608+25delinsGT	NP_001073291.1:n.1608+24_1608+25delinsGT
XM_005266981.2:c.1608+24_1608+25delinsGT	XP_005267038.1:n.1608+24_1608+25delinsGT
XM_005266982.2:c.1608+24_1608+25delinsGT	XP_005267039.1:n.1608+24_1608+25delinsGT
XM_011535820.1:c.1608+24_1608+25delinsGT	XP_011534122.1:n.1608+24_1608+25delinsGT
XM_005266981.3:c.1608+24_1608+25delinsGT	XP_005267038.1:n.1608+24_1608+25delinsGT
XM_005266982.3:c.1608+24_1608+25delinsGT	XP_005267039.1:n.1608+24_1608+25delinsGT
XM_011535820.2:c.1608+24_1608+25delinsGT	XP_011534122.1:n.1608+24_1608+25delinsGT
XM_017010851.2:c.1614+24_1614+25delinsGT	XP_016866340.1:n.1614+24_1614+25delinsGT
XM_017010853.1:c.1608+24_1608+25delinsGT	XP_016866342.1:n.1608+24_1608+25delinsGT
NM_000426.4:c.1608+24_1608+25delinsGT MANE Select	NP_000417.3:n.1608+24_1608+25delinsGT
NM_001079823.2:c.1608+24_1608+25delinsGT	NP_001073291.2:n.1608+24_1608+25delinsGT