Canonical Allele Identifier: CA451934052

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129802530G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481385G>A , CM000668.2:g.129481385G>A	GRCh38
NC_000006.11:g.129802530G>A , CM000668.1:g.129802530G>A	GRCh37
NC_000006.10:g.129844223G>A	NCBI36
NG_008678.1:g.603245G>A , LRG_409:g.603245G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7683G>A	ENSP00000481744.2:p.Leu2561=
ENST00000618192.5:c.7959G>A	ENSP00000480802.2:p.Leu2653=
ENST00000421865.3:c.7695G>A MANE Select	ENSP00000400365.2:p.Leu2565=
ENST00000421865.2:c.7695G>A	ENSP00000400365.2:p.Leu2565=
ENST00000617695.4:c.7683G>A	ENSP00000481744.1:p.Leu2561=
ENST00000618192.4:c.7692G>A	ENSP00000480802.1:p.Leu2564=
NM_000426.3:c.7695G>A , LRG_409t1:c.7695G>A	NP_000417.2:p.Leu2565=
NM_001079823.1:c.7683G>A	NP_001073291.1:p.Leu2561=
XM_005266981.2:c.7959G>A	XP_005267038.1:p.Leu2653=
XM_005266982.2:c.7947G>A	XP_005267039.1:p.Leu2649=
XM_011535820.1:c.7953G>A	XP_011534122.1:p.Leu2651=
XM_005266981.3:c.7959G>A	XP_005267038.1:p.Leu2653=
XM_005266982.3:c.7947G>A	XP_005267039.1:p.Leu2649=
XM_011535820.2:c.7953G>A	XP_011534122.1:p.Leu2651=
XM_017010851.2:c.7965G>A	XP_016866340.1:p.Leu2655=
XM_017010852.1:c.6090G>A	XP_016866341.1:p.Leu2030=
NM_000426.4:c.7695G>A MANE Select	NP_000417.3:p.Leu2565=
NM_001079823.2:c.7683G>A	NP_001073291.2:p.Leu2561=