Canonical Allele Identifier: CA2290334611

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928165T= , CM000680.2:g.23928165T=	GRCh38
NC_000018.9:g.21508129T= , CM000680.1:g.21508129T=	GRCh37
NC_000018.8:g.19762127T=	NCBI36
NG_007853.2:g.243568T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3393T= MANE Plus Clinical	ENSP00000269217.5:p.Asn1131=
ENST00000313654.14:c.8220T= MANE Select	ENSP00000324532.8:p.Asn2740=
ENST00000649721.1:c.4815T=	ENSP00000497885.1:p.Asn1605=
ENST00000269217.10:c.3393T=	ENSP00000269217.5:p.Asn1131=
ENST00000313654.13:c.8220T=	ENSP00000324532.8:p.Asn2740=
ENST00000399516.7:c.8052T=	ENSP00000382432.2:p.Asn2684=
ENST00000586751.5:c.2998T=
ENST00000587184.5:c.3225T=	ENSP00000466557.1:p.Asn1075=
ENST00000588770.5:n.2798T=
NM_000227.4:c.3393T=	NP_000218.3:p.Asn1131=
NM_001127717.2:c.8052T=	NP_001121189.2:p.Asn2684=
NM_001127718.2:c.3225T=	NP_001121190.2:p.Asn1075=
NM_198129.2:c.8220T=	NP_937762.2:p.Asn2740=
XM_011525978.1:c.8247T=	XP_011524280.1:p.Asn2749=
XM_011525979.1:c.8238T=	XP_011524281.1:p.Asn2746=
XM_011525980.1:c.8229T=	XP_011524282.1:p.Asn2743=
XM_011525981.1:c.8115T=	XP_011524283.1:p.Asn2705=
XM_011525982.1:c.7950T=	XP_011524284.1:p.Asn2650=
XM_011525978.2:c.8247T=	XP_011524280.1:p.Asn2749=
XM_011525979.2:c.8238T=	XP_011524281.1:p.Asn2746=
XM_011525980.2:c.8229T=	XP_011524282.1:p.Asn2743=
XM_011525981.2:c.8115T=	XP_011524283.1:p.Asn2705=
XM_011525982.2:c.7950T=	XP_011524284.1:p.Asn2650=
XM_017025743.1:c.6099T=	XP_016881232.1:p.Asn2033=
XM_017025744.1:c.3789T=	XP_016881233.1:p.Asn1263=
XR_001753199.1:n.8488T=
NM_000227.5:c.3393T=	NP_000218.3:p.Asn1131=
NM_001127717.3:c.8052T=	NP_001121189.2:p.Asn2684=
NM_001127718.3:c.3225T=	NP_001121190.2:p.Asn1075=
NM_198129.3:c.8220T=	NP_937762.2:p.Asn2740=
NM_000227.6:c.3393T= MANE Plus Clinical	NP_000218.3:p.Asn1131=
NM_001127717.4:c.8052T=	NP_001121189.2:p.Asn2684=
NM_001127718.4:c.3225T=	NP_001121190.2:p.Asn1075=
NM_198129.4:c.8220T= MANE Select	NP_937762.2:p.Asn2740=