Canonical Allele Identifier: CA402059335

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495361A>T (hg19) ; chr18:g.23915397A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915397A>T , CM000680.2:g.23915397A>T	GRCh38
NC_000018.9:g.21495361A>T , CM000680.1:g.21495361A>T	GRCh37
NC_000018.8:g.19749359A>T	NCBI36
NG_007853.2:g.230800A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2926A>T MANE Plus Clinical	ENSP00000269217.5:p.Thr976Ser
ENST00000313654.14:c.7753A>T MANE Select	ENSP00000324532.8:p.Thr2585Ser
ENST00000649721.1:c.4348A>T	ENSP00000497885.1:p.Thr1450Ser
ENST00000269217.10:c.2926A>T	ENSP00000269217.5:p.Thr976Ser
ENST00000313654.13:c.7753A>T	ENSP00000324532.8:p.Thr2585Ser
ENST00000399516.7:c.7585A>T	ENSP00000382432.2:p.Thr2529Ser
ENST00000586751.5:c.2531A>T
ENST00000587184.5:c.2758A>T	ENSP00000466557.1:p.Thr920Ser
ENST00000588770.5:n.2331A>T
NM_000227.4:c.2926A>T	NP_000218.3:p.Thr976Ser
NM_001127717.2:c.7585A>T	NP_001121189.2:p.Thr2529Ser
NM_001127718.2:c.2758A>T	NP_001121190.2:p.Thr920Ser
NM_198129.2:c.7753A>T	NP_937762.2:p.Thr2585Ser
XM_011525978.1:c.7780A>T	XP_011524280.1:p.Thr2594Ser
XM_011525979.1:c.7771A>T	XP_011524281.1:p.Thr2591Ser
XM_011525980.1:c.7762A>T	XP_011524282.1:p.Thr2588Ser
XM_011525981.1:c.7648A>T	XP_011524283.1:p.Thr2550Ser
XM_011525982.1:c.7483A>T	XP_011524284.1:p.Thr2495Ser
XM_011525978.2:c.7780A>T	XP_011524280.1:p.Thr2594Ser
XM_011525979.2:c.7771A>T	XP_011524281.1:p.Thr2591Ser
XM_011525980.2:c.7762A>T	XP_011524282.1:p.Thr2588Ser
XM_011525981.2:c.7648A>T	XP_011524283.1:p.Thr2550Ser
XM_011525982.2:c.7483A>T	XP_011524284.1:p.Thr2495Ser
XM_017025743.1:c.5632A>T	XP_016881232.1:p.Thr1878Ser
XM_017025744.1:c.3322A>T	XP_016881233.1:p.Thr1108Ser
XR_001753199.1:n.8021A>T
NM_000227.5:c.2926A>T	NP_000218.3:p.Thr976Ser
NM_001127717.3:c.7585A>T	NP_001121189.2:p.Thr2529Ser
NM_001127718.3:c.2758A>T	NP_001121190.2:p.Thr920Ser
NM_198129.3:c.7753A>T	NP_937762.2:p.Thr2585Ser
NM_000227.6:c.2926A>T MANE Plus Clinical	NP_000218.3:p.Thr976Ser
NM_001127717.4:c.7585A>T	NP_001121189.2:p.Thr2529Ser
NM_001127718.4:c.2758A>T	NP_001121190.2:p.Thr920Ser
NM_198129.4:c.7753A>T MANE Select	NP_937762.2:p.Thr2585Ser