Canonical Allele Identifier: CA2290334610

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928164A= , CM000680.2:g.23928164A=	GRCh38
NC_000018.9:g.21508128A= , CM000680.1:g.21508128A=	GRCh37
NC_000018.8:g.19762126A=	NCBI36
NG_007853.2:g.243567A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3392A= MANE Plus Clinical	ENSP00000269217.5:p.Asn1131=
ENST00000313654.14:c.8219A= MANE Select	ENSP00000324532.8:p.Asn2740=
ENST00000649721.1:c.4814A=	ENSP00000497885.1:p.Asn1605=
ENST00000269217.10:c.3392A=	ENSP00000269217.5:p.Asn1131=
ENST00000313654.13:c.8219A=	ENSP00000324532.8:p.Asn2740=
ENST00000399516.7:c.8051A=	ENSP00000382432.2:p.Asn2684=
ENST00000586751.5:c.2997A=
ENST00000587184.5:c.3224A=	ENSP00000466557.1:p.Asn1075=
ENST00000588770.5:n.2797A=
NM_000227.4:c.3392A=	NP_000218.3:p.Asn1131=
NM_001127717.2:c.8051A=	NP_001121189.2:p.Asn2684=
NM_001127718.2:c.3224A=	NP_001121190.2:p.Asn1075=
NM_198129.2:c.8219A=	NP_937762.2:p.Asn2740=
XM_011525978.1:c.8246A=	XP_011524280.1:p.Asn2749=
XM_011525979.1:c.8237A=	XP_011524281.1:p.Asn2746=
XM_011525980.1:c.8228A=	XP_011524282.1:p.Asn2743=
XM_011525981.1:c.8114A=	XP_011524283.1:p.Asn2705=
XM_011525982.1:c.7949A=	XP_011524284.1:p.Asn2650=
XM_011525978.2:c.8246A=	XP_011524280.1:p.Asn2749=
XM_011525979.2:c.8237A=	XP_011524281.1:p.Asn2746=
XM_011525980.2:c.8228A=	XP_011524282.1:p.Asn2743=
XM_011525981.2:c.8114A=	XP_011524283.1:p.Asn2705=
XM_011525982.2:c.7949A=	XP_011524284.1:p.Asn2650=
XM_017025743.1:c.6098A=	XP_016881232.1:p.Asn2033=
XM_017025744.1:c.3788A=	XP_016881233.1:p.Asn1263=
XR_001753199.1:n.8487A=
NM_000227.5:c.3392A=	NP_000218.3:p.Asn1131=
NM_001127717.3:c.8051A=	NP_001121189.2:p.Asn2684=
NM_001127718.3:c.3224A=	NP_001121190.2:p.Asn1075=
NM_198129.3:c.8219A=	NP_937762.2:p.Asn2740=
NM_000227.6:c.3392A= MANE Plus Clinical	NP_000218.3:p.Asn1131=
NM_001127717.4:c.8051A=	NP_001121189.2:p.Asn2684=
NM_001127718.4:c.3224A=	NP_001121190.2:p.Asn1075=
NM_198129.4:c.8219A= MANE Select	NP_937762.2:p.Asn2740=