Canonical Allele Identifier: CA365628305

Gene: LAMA2

Linked Data

• gnomAD v4: 6-129481395-G-T
• MyVariant Identifiers: chr6:g.129802540G>T (hg19) ; chr6:g.129481395G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481395G>T , CM000668.2:g.129481395G>T	GRCh38
NC_000006.11:g.129802540G>T , CM000668.1:g.129802540G>T	GRCh37
NC_000006.10:g.129844233G>T	NCBI36
NG_008678.1:g.603255G>T , LRG_409:g.603255G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7693G>T	ENSP00000481744.2:p.Gly2565Trp
ENST00000618192.5:c.7969G>T	ENSP00000480802.2:p.Gly2657Trp
ENST00000421865.3:c.7705G>T MANE Select	ENSP00000400365.2:p.Gly2569Trp
ENST00000421865.2:c.7705G>T	ENSP00000400365.2:p.Gly2569Trp
ENST00000617695.4:c.7693G>T	ENSP00000481744.1:p.Gly2565Trp
ENST00000618192.4:c.7702G>T	ENSP00000480802.1:p.Gly2568Trp
NM_000426.3:c.7705G>T , LRG_409t1:c.7705G>T	NP_000417.2:p.Gly2569Trp
NM_001079823.1:c.7693G>T	NP_001073291.1:p.Gly2565Trp
XM_005266981.2:c.7969G>T	XP_005267038.1:p.Gly2657Trp
XM_005266982.2:c.7957G>T	XP_005267039.1:p.Gly2653Trp
XM_011535820.1:c.7963G>T	XP_011534122.1:p.Gly2655Trp
XM_005266981.3:c.7969G>T	XP_005267038.1:p.Gly2657Trp
XM_005266982.3:c.7957G>T	XP_005267039.1:p.Gly2653Trp
XM_011535820.2:c.7963G>T	XP_011534122.1:p.Gly2655Trp
XM_017010851.2:c.7975G>T	XP_016866340.1:p.Gly2659Trp
XM_017010852.1:c.6100G>T	XP_016866341.1:p.Gly2034Trp
NM_000426.4:c.7705G>T MANE Select	NP_000417.3:p.Gly2569Trp
NM_001079823.2:c.7693G>T	NP_001073291.2:p.Gly2565Trp