Canonical Allele Identifier: CA2290343874

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23949910G= , CM000680.2:g.23949910G=	GRCh38
NC_000018.9:g.21529874G= , CM000680.1:g.21529874G=	GRCh37
NC_000018.8:g.19783872G=	NCBI36
NG_007853.2:g.265313G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4670G= MANE Plus Clinical	ENSP00000269217.5:p.Gly1557=
ENST00000313654.14:c.9497G= MANE Select	ENSP00000324532.8:p.Gly3166=
ENST00000649721.1:c.6092G=	ENSP00000497885.1:p.Gly2031=
ENST00000269217.10:c.4670G=	ENSP00000269217.5:p.Gly1557=
ENST00000313654.13:c.9497G=	ENSP00000324532.8:p.Gly3166=
ENST00000399516.7:c.9329G=	ENSP00000382432.2:p.Gly3110=
ENST00000587184.5:c.4502G=	ENSP00000466557.1:p.Gly1501=
ENST00000588004.1:c.18G=
ENST00000588770.5:n.4075G=
NM_000227.4:c.4670G=	NP_000218.3:p.Gly1557=
NM_001127717.2:c.9329G=	NP_001121189.2:p.Gly3110=
NM_001127718.2:c.4502G=	NP_001121190.2:p.Gly1501=
NM_198129.2:c.9497G=	NP_937762.2:p.Gly3166=
XM_011525978.1:c.9524G=	XP_011524280.1:p.Gly3175=
XM_011525979.1:c.9515G=	XP_011524281.1:p.Gly3172=
XM_011525980.1:c.9506G=	XP_011524282.1:p.Gly3169=
XM_011525981.1:c.9392G=	XP_011524283.1:p.Gly3131=
XM_011525982.1:c.9227G=	XP_011524284.1:p.Gly3076=
XM_011525978.2:c.9524G=	XP_011524280.1:p.Gly3175=
XM_011525979.2:c.9515G=	XP_011524281.1:p.Gly3172=
XM_011525980.2:c.9506G=	XP_011524282.1:p.Gly3169=
XM_011525981.2:c.9392G=	XP_011524283.1:p.Gly3131=
XM_011525982.2:c.9227G=	XP_011524284.1:p.Gly3076=
XM_017025743.1:c.7376G=	XP_016881232.1:p.Gly2459=
XM_017025744.1:c.5066G=	XP_016881233.1:p.Gly1689=
XR_001753199.1:n.9765G=
NM_000227.5:c.4670G=	NP_000218.3:p.Gly1557=
NM_001127717.3:c.9329G=	NP_001121189.2:p.Gly3110=
NM_001127718.3:c.4502G=	NP_001121190.2:p.Gly1501=
NM_198129.3:c.9497G=	NP_937762.2:p.Gly3166=
NM_000227.6:c.4670G= MANE Plus Clinical	NP_000218.3:p.Gly1557=
NM_001127717.4:c.9329G=	NP_001121189.2:p.Gly3110=
NM_001127718.4:c.4502G=	NP_001121190.2:p.Gly1501=
NM_198129.4:c.9497G= MANE Select	NP_937762.2:p.Gly3166=