Canonical Allele Identifier: CA365619030

Gene: LAMA2

Linked Data

• dbSNP Id: rs1385528581
• MyVariant Identifiers: chr6:g.129781348G>T (hg19) ; chr6:g.129460203G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129460203G>T , CM000668.2:g.129460203G>T	GRCh38
NC_000006.11:g.129781348G>T , CM000668.1:g.129781348G>T	GRCh37
NC_000006.10:g.129823041G>T	NCBI36
NG_008678.1:g.582063G>T , LRG_409:g.582063G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.6871G>T	ENSP00000481744.2:p.Ala2291Ser
ENST00000618192.5:c.7135G>T	ENSP00000480802.2:p.Ala2379Ser
ENST00000684985.1:n.502G>T
ENST00000688150.1:n.210G>T
ENST00000421865.3:c.6871G>T MANE Select	ENSP00000400365.2:p.Ala2291Ser
ENST00000421865.2:c.6871G>T	ENSP00000400365.2:p.Ala2291Ser
ENST00000617695.4:c.6871G>T	ENSP00000481744.1:p.Ala2291Ser
ENST00000618192.4:c.6868G>T	ENSP00000480802.1:p.Ala2290Ser
NM_000426.3:c.6871G>T , LRG_409t1:c.6871G>T	NP_000417.2:p.Ala2291Ser
NM_001079823.1:c.6871G>T	NP_001073291.1:p.Ala2291Ser
XM_005266981.2:c.7135G>T	XP_005267038.1:p.Ala2379Ser
XM_005266982.2:c.7135G>T	XP_005267039.1:p.Ala2379Ser
XM_011535820.1:c.7129G>T	XP_011534122.1:p.Ala2377Ser
XM_005266981.3:c.7135G>T	XP_005267038.1:p.Ala2379Ser
XM_005266982.3:c.7135G>T	XP_005267039.1:p.Ala2379Ser
XM_011535820.2:c.7129G>T	XP_011534122.1:p.Ala2377Ser
XM_017010851.2:c.7141G>T	XP_016866340.1:p.Ala2381Ser
XM_017010852.1:c.5266G>T	XP_016866341.1:p.Ala1756Ser
NM_000426.4:c.6871G>T MANE Select	NP_000417.3:p.Ala2291Ser
NM_001079823.2:c.6871G>T	NP_001073291.2:p.Ala2291Ser