Canonical Allele Identifier: CA2680308038

Gene: LAMA2

Linked Data

• gnomAD v4: 6-129465352-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129465353_129465354dup , CM000668.2:g.129465353_129465354dup	GRCh38
NC_000006.11:g.129786498_129786499dup , CM000668.1:g.129786498_129786499dup	GRCh37
NC_000006.10:g.129828191_129828192dup	NCBI36
NG_008678.1:g.587213_587214dup , LRG_409:g.587213_587214dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7300+64_7300+65dup	ENSP00000481744.2:n.7300+64_7300+65dup
ENST00000618192.5:c.7564+64_7564+65dup	ENSP00000480802.2:n.7564+64_7564+65dup
ENST00000684985.1:n.931+64_931+65dup
ENST00000421865.3:c.7300+64_7300+65dup MANE Select	ENSP00000400365.2:n.7300+64_7300+65dup
ENST00000421865.2:c.7300+64_7300+65dup	ENSP00000400365.2:n.7300+64_7300+65dup
ENST00000617695.4:c.7300+64_7300+65dup	ENSP00000481744.1:n.7300+64_7300+65dup
ENST00000618192.4:c.7297+64_7297+65dup	ENSP00000480802.1:n.7297+64_7297+65dup
NM_000426.3:c.7300+64_7300+65dup , LRG_409t1:c.7300+64_7300+65dup	NP_000417.2:n.7300+64_7300+65dup
NM_001079823.1:c.7300+64_7300+65dup	NP_001073291.1:n.7300+64_7300+65dup
XM_005266981.2:c.7564+64_7564+65dup	XP_005267038.1:n.7564+64_7564+65dup
XM_005266982.2:c.7564+64_7564+65dup	XP_005267039.1:n.7564+64_7564+65dup
XM_011535820.1:c.7558+64_7558+65dup	XP_011534122.1:n.7558+64_7558+65dup
XM_005266981.3:c.7564+64_7564+65dup	XP_005267038.1:n.7564+64_7564+65dup
XM_005266982.3:c.7564+64_7564+65dup	XP_005267039.1:n.7564+64_7564+65dup
XM_011535820.2:c.7558+64_7558+65dup	XP_011534122.1:n.7558+64_7558+65dup
XM_017010851.2:c.7570+64_7570+65dup	XP_016866340.1:n.7570+64_7570+65dup
XM_017010852.1:c.5695+64_5695+65dup	XP_016866341.1:n.5695+64_5695+65dup
NM_000426.4:c.7300+64_7300+65dup MANE Select	NP_000417.3:n.7300+64_7300+65dup
NM_001079823.2:c.7300+64_7300+65dup	NP_001073291.2:n.7300+64_7300+65dup