Canonical Allele Identifier: CA2290310944

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23873003G= , CM000680.2:g.23873003G=	GRCh38
NC_000018.9:g.21452967G= , CM000680.1:g.21452967G=	GRCh37
NC_000018.8:g.19706965G=	NCBI36
NG_007853.2:g.188406G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313654.14:c.4998+1342G= MANE Select	ENSP00000324532.8:n.4998+1342G=
ENST00000649721.1:c.1890+1342G=	ENSP00000497885.1:n.1890+1342G=
ENST00000269217.10:c.-42G=	ENSP00000269217.5:n.-42G=
ENST00000313654.13:c.4998+1342G=	ENSP00000324532.8:n.4998+1342G=
ENST00000399516.7:c.4998+1342G=	ENSP00000382432.2:n.4998+1342G=
NM_001127717.2:c.4998+1342G=	NP_001121189.2:n.4998+1342G=
NM_198129.2:c.4998+1342G=	NP_937762.2:n.4998+1342G=
XM_011525978.1:c.5025+1342G=	XP_011524280.1:n.5025+1342G=
XM_011525979.1:c.5016+1342G=	XP_011524281.1:n.5016+1342G=
XM_011525980.1:c.5007+1342G=	XP_011524282.1:n.5007+1342G=
XM_011525981.1:c.4893+1342G=	XP_011524283.1:n.4893+1342G=
XM_011525982.1:c.5025+1342G=	XP_011524284.1:n.5025+1342G=
XM_011525978.2:c.5025+1342G=	XP_011524280.1:n.5025+1342G=
XM_011525979.2:c.5016+1342G=	XP_011524281.1:n.5016+1342G=
XM_011525980.2:c.5007+1342G=	XP_011524282.1:n.5007+1342G=
XM_011525981.2:c.4893+1342G=	XP_011524283.1:n.4893+1342G=
XM_011525982.2:c.5025+1342G=	XP_011524284.1:n.5025+1342G=
XM_017025743.1:c.2877+1342G=	XP_016881232.1:n.2877+1342G=
XM_017025744.1:c.567+1342G=	XP_016881233.1:n.567+1342G=
XR_001753199.1:n.5266+1342G=
NM_001127717.3:c.4998+1342G=	NP_001121189.2:n.4998+1342G=
NM_198129.3:c.4998+1342G=	NP_937762.2:n.4998+1342G=
NM_001127717.4:c.4998+1342G=	NP_001121189.2:n.4998+1342G=
NM_198129.4:c.4998+1342G= MANE Select	NP_937762.2:n.4998+1342G=