Canonical Allele Identifier: CA402052007

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21530056C>G (hg19) ; chr18:g.23950092C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950092C>G , CM000680.2:g.23950092C>G	GRCh38
NC_000018.9:g.21530056C>G , CM000680.1:g.21530056C>G	GRCh37
NC_000018.8:g.19784054C>G	NCBI36
NG_007853.2:g.265495C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4748C>G MANE Plus Clinical	ENSP00000269217.5:p.Thr1583Ser
ENST00000313654.14:c.9575C>G MANE Select	ENSP00000324532.8:p.Thr3192Ser
ENST00000649721.1:c.6170C>G	ENSP00000497885.1:p.Thr2057Ser
ENST00000269217.10:c.4748C>G	ENSP00000269217.5:p.Thr1583Ser
ENST00000313654.13:c.9575C>G	ENSP00000324532.8:p.Thr3192Ser
ENST00000399516.7:c.9407C>G	ENSP00000382432.2:p.Thr3136Ser
ENST00000587184.5:c.4580C>G	ENSP00000466557.1:p.Thr1527Ser
ENST00000588004.1:c.96C>G
ENST00000588770.5:n.4153C>G
NM_000227.4:c.4748C>G	NP_000218.3:p.Thr1583Ser
NM_001127717.2:c.9407C>G	NP_001121189.2:p.Thr3136Ser
NM_001127718.2:c.4580C>G	NP_001121190.2:p.Thr1527Ser
NM_198129.2:c.9575C>G	NP_937762.2:p.Thr3192Ser
XM_011525978.1:c.9602C>G	XP_011524280.1:p.Thr3201Ser
XM_011525979.1:c.9593C>G	XP_011524281.1:p.Thr3198Ser
XM_011525980.1:c.9584C>G	XP_011524282.1:p.Thr3195Ser
XM_011525981.1:c.9470C>G	XP_011524283.1:p.Thr3157Ser
XM_011525982.1:c.9305C>G	XP_011524284.1:p.Thr3102Ser
XM_011525978.2:c.9602C>G	XP_011524280.1:p.Thr3201Ser
XM_011525979.2:c.9593C>G	XP_011524281.1:p.Thr3198Ser
XM_011525980.2:c.9584C>G	XP_011524282.1:p.Thr3195Ser
XM_011525981.2:c.9470C>G	XP_011524283.1:p.Thr3157Ser
XM_011525982.2:c.9305C>G	XP_011524284.1:p.Thr3102Ser
XM_017025743.1:c.7454C>G	XP_016881232.1:p.Thr2485Ser
XM_017025744.1:c.5144C>G	XP_016881233.1:p.Thr1715Ser
XR_001753199.1:n.9843C>G
NM_000227.5:c.4748C>G	NP_000218.3:p.Thr1583Ser
NM_001127717.3:c.9407C>G	NP_001121189.2:p.Thr3136Ser
NM_001127718.3:c.4580C>G	NP_001121190.2:p.Thr1527Ser
NM_198129.3:c.9575C>G	NP_937762.2:p.Thr3192Ser
NM_000227.6:c.4748C>G MANE Plus Clinical	NP_000218.3:p.Thr1583Ser
NM_001127717.4:c.9407C>G	NP_001121189.2:p.Thr3136Ser
NM_001127718.4:c.4580C>G	NP_001121190.2:p.Thr1527Ser
NM_198129.4:c.9575C>G MANE Select	NP_937762.2:p.Thr3192Ser