Canonical Allele Identifier: CA2290324116

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903339G= , CM000680.2:g.23903339G=	GRCh38
NC_000018.9:g.21483303G= , CM000680.1:g.21483303G=	GRCh37
NC_000018.8:g.19737301G=	NCBI36
NG_007853.2:g.218742G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1491+214G= MANE Plus Clinical	ENSP00000269217.5:n.1491+214G=
ENST00000313654.14:c.6318+214G= MANE Select	ENSP00000324532.8:n.6318+214G=
ENST00000649721.1:c.3210+214G=	ENSP00000497885.1:n.3210+214G=
ENST00000269217.10:c.1491+214G=	ENSP00000269217.5:n.1491+214G=
ENST00000313654.13:c.6318+214G=	ENSP00000324532.8:n.6318+214G=
ENST00000399516.7:c.6150+214G=	ENSP00000382432.2:n.6150+214G=
ENST00000586751.5:c.1096+214G=
ENST00000587184.5:c.1323+214G=	ENSP00000466557.1:n.1323+214G=
ENST00000588770.5:n.896+214G=
NM_000227.4:c.1491+214G=	NP_000218.3:n.1491+214G=
NM_001127717.2:c.6150+214G=	NP_001121189.2:n.6150+214G=
NM_001127718.2:c.1323+214G=	NP_001121190.2:n.1323+214G=
NM_198129.2:c.6318+214G=	NP_937762.2:n.6318+214G=
XM_011525978.1:c.6345+214G=	XP_011524280.1:n.6345+214G=
XM_011525979.1:c.6336+214G=	XP_011524281.1:n.6336+214G=
XM_011525980.1:c.6327+214G=	XP_011524282.1:n.6327+214G=
XM_011525981.1:c.6213+214G=	XP_011524283.1:n.6213+214G=
XM_011525982.1:c.6345+214G=	XP_011524284.1:n.6345+214G=
XM_011525978.2:c.6345+214G=	XP_011524280.1:n.6345+214G=
XM_011525979.2:c.6336+214G=	XP_011524281.1:n.6336+214G=
XM_011525980.2:c.6327+214G=	XP_011524282.1:n.6327+214G=
XM_011525981.2:c.6213+214G=	XP_011524283.1:n.6213+214G=
XM_011525982.2:c.6345+214G=	XP_011524284.1:n.6345+214G=
XM_017025743.1:c.4197+214G=	XP_016881232.1:n.4197+214G=
XM_017025744.1:c.1887+214G=	XP_016881233.1:n.1887+214G=
XR_001753199.1:n.6586+214G=
NM_000227.5:c.1491+214G=	NP_000218.3:n.1491+214G=
NM_001127717.3:c.6150+214G=	NP_001121189.2:n.6150+214G=
NM_001127718.3:c.1323+214G=	NP_001121190.2:n.1323+214G=
NM_198129.3:c.6318+214G=	NP_937762.2:n.6318+214G=
NM_000227.6:c.1491+214G= MANE Plus Clinical	NP_000218.3:n.1491+214G=
NM_001127717.4:c.6150+214G=	NP_001121189.2:n.6150+214G=
NM_001127718.4:c.1323+214G=	NP_001121190.2:n.1323+214G=
NM_198129.4:c.6318+214G= MANE Select	NP_937762.2:n.6318+214G=