Canonical Allele Identifier: CA365623875

Gene: LAMA2

Linked Data

• dbSNP Id: rs1486292247
• gnomAD v3: 6-129427756-C-G
• gnomAD v4: 6-129427756-C-G
• MyVariant Identifiers: chr6:g.129748901C>G (hg19) ; chr6:g.129427756C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129427756C>G , CM000668.2:g.129427756C>G	GRCh38
NC_000006.11:g.129748901C>G , CM000668.1:g.129748901C>G	GRCh37
NC_000006.10:g.129790594C>G	NCBI36
NG_008678.1:g.549616C>G , LRG_409:g.549616C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000617695.5:c.5870C>G	ENSP00000481744.2:p.Thr1957Arg
ENST00000618192.5:c.6134C>G	ENSP00000480802.2:p.Thr2045Arg
ENST00000421865.3:c.5870C>G MANE Select	ENSP00000400365.2:p.Thr1957Arg
ENST00000421865.2:c.5870C>G	ENSP00000400365.2:p.Thr1957Arg
ENST00000617695.4:c.5870C>G	ENSP00000481744.1:p.Thr1957Arg
ENST00000618192.4:c.5870C>G	ENSP00000480802.1:p.Thr1957Arg
NM_000426.3:c.5870C>G , LRG_409t1:c.5870C>G	NP_000417.2:p.Thr1957Arg
NM_001079823.1:c.5870C>G	NP_001073291.1:p.Thr1957Arg
XM_005266981.2:c.6134C>G	XP_005267038.1:p.Thr2045Arg
XM_005266982.2:c.6134C>G	XP_005267039.1:p.Thr2045Arg
XM_011535820.1:c.6134C>G	XP_011534122.1:p.Thr2045Arg
XM_005266981.3:c.6134C>G	XP_005267038.1:p.Thr2045Arg
XM_005266982.3:c.6134C>G	XP_005267039.1:p.Thr2045Arg
XM_011535820.2:c.6134C>G	XP_011534122.1:p.Thr2045Arg
XM_017010851.2:c.6140C>G	XP_016866340.1:p.Thr2047Arg
XM_017010852.1:c.4265C>G	XP_016866341.1:p.Thr1422Arg
NM_000426.4:c.5870C>G MANE Select	NP_000417.3:p.Thr1957Arg
NM_001079823.2:c.5870C>G	NP_001073291.2:p.Thr1957Arg