Canonical Allele Identifier: CA503331896

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21478785T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898821T>C , CM000680.2:g.23898821T>C	GRCh38
NC_000018.9:g.21478785T>C , CM000680.1:g.21478785T>C	GRCh37
NC_000018.8:g.19732783T>C	NCBI36
NG_007853.2:g.214224T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.870T>C MANE Plus Clinical	ENSP00000269217.5:p.Asn290=
ENST00000313654.14:c.5697T>C MANE Select	ENSP00000324532.8:p.Asn1899=
ENST00000649721.1:c.2589T>C	ENSP00000497885.1:p.Asn863=
ENST00000269217.10:c.870T>C	ENSP00000269217.5:p.Asn290=
ENST00000313654.13:c.5697T>C	ENSP00000324532.8:p.Asn1899=
ENST00000399516.7:c.5697T>C	ENSP00000382432.2:p.Asn1899=
ENST00000586709.1:n.85T>C
ENST00000586751.5:c.475T>C
ENST00000587184.5:c.870T>C	ENSP00000466557.1:p.Asn290=
ENST00000588770.5:n.275T>C
NM_000227.4:c.870T>C	NP_000218.3:p.Asn290=
NM_001127717.2:c.5697T>C	NP_001121189.2:p.Asn1899=
NM_001127718.2:c.870T>C	NP_001121190.2:p.Asn290=
NM_198129.2:c.5697T>C	NP_937762.2:p.Asn1899=
XM_011525978.1:c.5724T>C	XP_011524280.1:p.Asn1908=
XM_011525979.1:c.5715T>C	XP_011524281.1:p.Asn1905=
XM_011525980.1:c.5706T>C	XP_011524282.1:p.Asn1902=
XM_011525981.1:c.5592T>C	XP_011524283.1:p.Asn1864=
XM_011525982.1:c.5724T>C	XP_011524284.1:p.Asn1908=
XM_011525978.2:c.5724T>C	XP_011524280.1:p.Asn1908=
XM_011525979.2:c.5715T>C	XP_011524281.1:p.Asn1905=
XM_011525980.2:c.5706T>C	XP_011524282.1:p.Asn1902=
XM_011525981.2:c.5592T>C	XP_011524283.1:p.Asn1864=
XM_011525982.2:c.5724T>C	XP_011524284.1:p.Asn1908=
XM_017025743.1:c.3576T>C	XP_016881232.1:p.Asn1192=
XM_017025744.1:c.1266T>C	XP_016881233.1:p.Asn422=
XR_001753199.1:n.5965T>C
NM_000227.5:c.870T>C	NP_000218.3:p.Asn290=
NM_001127717.3:c.5697T>C	NP_001121189.2:p.Asn1899=
NM_001127718.3:c.870T>C	NP_001121190.2:p.Asn290=
NM_198129.3:c.5697T>C	NP_937762.2:p.Asn1899=
NM_000227.6:c.870T>C MANE Plus Clinical	NP_000218.3:p.Asn290=
NM_001127717.4:c.5697T>C	NP_001121189.2:p.Asn1899=
NM_001127718.4:c.870T>C	NP_001121190.2:p.Asn290=
NM_198129.4:c.5697T>C MANE Select	NP_937762.2:p.Asn1899=