Canonical Allele Identifier: CA365628441

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129802577C>A (hg19) ; chr6:g.129481432C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481432C>A , CM000668.2:g.129481432C>A	GRCh38
NC_000006.11:g.129802577C>A , CM000668.1:g.129802577C>A	GRCh37
NC_000006.10:g.129844270C>A	NCBI36
NG_008678.1:g.603292C>A , LRG_409:g.603292C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7730C>A	ENSP00000481744.2:p.Thr2577Asn
ENST00000618192.5:c.8006C>A	ENSP00000480802.2:p.Thr2669Asn
ENST00000421865.3:c.7742C>A MANE Select	ENSP00000400365.2:p.Thr2581Asn
ENST00000421865.2:c.7742C>A	ENSP00000400365.2:p.Thr2581Asn
ENST00000617695.4:c.7730C>A	ENSP00000481744.1:p.Thr2577Asn
ENST00000618192.4:c.7739C>A	ENSP00000480802.1:p.Thr2580Asn
NM_000426.3:c.7742C>A , LRG_409t1:c.7742C>A	NP_000417.2:p.Thr2581Asn
NM_001079823.1:c.7730C>A	NP_001073291.1:p.Thr2577Asn
XM_005266981.2:c.8006C>A	XP_005267038.1:p.Thr2669Asn
XM_005266982.2:c.7994C>A	XP_005267039.1:p.Thr2665Asn
XM_011535820.1:c.8000C>A	XP_011534122.1:p.Thr2667Asn
XM_005266981.3:c.8006C>A	XP_005267038.1:p.Thr2669Asn
XM_005266982.3:c.7994C>A	XP_005267039.1:p.Thr2665Asn
XM_011535820.2:c.8000C>A	XP_011534122.1:p.Thr2667Asn
XM_017010851.2:c.8012C>A	XP_016866340.1:p.Thr2671Asn
XM_017010852.1:c.6137C>A	XP_016866341.1:p.Thr2046Asn
NM_000426.4:c.7742C>A MANE Select	NP_000417.3:p.Thr2581Asn
NM_001079823.2:c.7730C>A	NP_001073291.2:p.Thr2577Asn