Canonical Allele Identifier: CA451934125

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129802578T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481433T>G , CM000668.2:g.129481433T>G	GRCh38
NC_000006.11:g.129802578T>G , CM000668.1:g.129802578T>G	GRCh37
NC_000006.10:g.129844271T>G	NCBI36
NG_008678.1:g.603293T>G , LRG_409:g.603293T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7731T>G	ENSP00000481744.2:p.Thr2577=
ENST00000618192.5:c.8007T>G	ENSP00000480802.2:p.Thr2669=
ENST00000421865.3:c.7743T>G MANE Select	ENSP00000400365.2:p.Thr2581=
ENST00000421865.2:c.7743T>G	ENSP00000400365.2:p.Thr2581=
ENST00000617695.4:c.7731T>G	ENSP00000481744.1:p.Thr2577=
ENST00000618192.4:c.7740T>G	ENSP00000480802.1:p.Thr2580=
NM_000426.3:c.7743T>G , LRG_409t1:c.7743T>G	NP_000417.2:p.Thr2581=
NM_001079823.1:c.7731T>G	NP_001073291.1:p.Thr2577=
XM_005266981.2:c.8007T>G	XP_005267038.1:p.Thr2669=
XM_005266982.2:c.7995T>G	XP_005267039.1:p.Thr2665=
XM_011535820.1:c.8001T>G	XP_011534122.1:p.Thr2667=
XM_005266981.3:c.8007T>G	XP_005267038.1:p.Thr2669=
XM_005266982.3:c.7995T>G	XP_005267039.1:p.Thr2665=
XM_011535820.2:c.8001T>G	XP_011534122.1:p.Thr2667=
XM_017010851.2:c.8013T>G	XP_016866340.1:p.Thr2671=
XM_017010852.1:c.6138T>G	XP_016866341.1:p.Thr2046=
NM_000426.4:c.7743T>G MANE Select	NP_000417.3:p.Thr2581=
NM_001079823.2:c.7731T>G	NP_001073291.2:p.Thr2577=