Canonical Allele Identifier: CA2290329001

Gene: LAMA3

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2926A= MANE Plus Clinical	ENSP00000269217.5:p.Thr976=
ENST00000313654.14:c.7753A= MANE Select	ENSP00000324532.8:p.Thr2585=
ENST00000649721.1:c.4348A=	ENSP00000497885.1:p.Thr1450=
ENST00000269217.10:c.2926A=	ENSP00000269217.5:p.Thr976=
ENST00000313654.13:c.7753A=	ENSP00000324532.8:p.Thr2585=
ENST00000399516.7:c.7585A=	ENSP00000382432.2:p.Thr2529=
ENST00000586751.5:c.2531A=
ENST00000587184.5:c.2758A=	ENSP00000466557.1:p.Thr920=
ENST00000588770.5:n.2331A=
NM_000227.4:c.2926A=	NP_000218.3:p.Thr976=
NM_001127717.2:c.7585A=	NP_001121189.2:p.Thr2529=
NM_001127718.2:c.2758A=	NP_001121190.2:p.Thr920=
NM_198129.2:c.7753A=	NP_937762.2:p.Thr2585=
XM_011525978.1:c.7780A=	XP_011524280.1:p.Thr2594=
XM_011525979.1:c.7771A=	XP_011524281.1:p.Thr2591=
XM_011525980.1:c.7762A=	XP_011524282.1:p.Thr2588=
XM_011525981.1:c.7648A=	XP_011524283.1:p.Thr2550=
XM_011525982.1:c.7483A=	XP_011524284.1:p.Thr2495=
XM_011525978.2:c.7780A=	XP_011524280.1:p.Thr2594=
XM_011525979.2:c.7771A=	XP_011524281.1:p.Thr2591=
XM_011525980.2:c.7762A=	XP_011524282.1:p.Thr2588=
XM_011525981.2:c.7648A=	XP_011524283.1:p.Thr2550=
XM_011525982.2:c.7483A=	XP_011524284.1:p.Thr2495=
XM_017025743.1:c.5632A=	XP_016881232.1:p.Thr1878=
XM_017025744.1:c.3322A=	XP_016881233.1:p.Thr1108=
XR_001753199.1:n.8021A=
NM_000227.5:c.2926A=	NP_000218.3:p.Thr976=
NM_001127717.3:c.7585A=	NP_001121189.2:p.Thr2529=
NM_001127718.3:c.2758A=	NP_001121190.2:p.Thr920=
NM_198129.3:c.7753A=	NP_937762.2:p.Thr2585=
NM_000227.6:c.2926A= MANE Plus Clinical	NP_000218.3:p.Thr976=
NM_001127717.4:c.7585A=	NP_001121189.2:p.Thr2529=
NM_001127718.4:c.2758A=	NP_001121190.2:p.Thr920=
NM_198129.4:c.7753A= MANE Select	NP_937762.2:p.Thr2585=