Canonical Allele Identifier: CA503331857

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21478728C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898764C>A , CM000680.2:g.23898764C>A	GRCh38
NC_000018.9:g.21478728C>A , CM000680.1:g.21478728C>A	GRCh37
NC_000018.8:g.19732726C>A	NCBI36
NG_007853.2:g.214167C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.813C>A MANE Plus Clinical	ENSP00000269217.5:p.Ala271=
ENST00000313654.14:c.5640C>A MANE Select	ENSP00000324532.8:p.Ala1880=
ENST00000649721.1:c.2532C>A	ENSP00000497885.1:p.Ala844=
ENST00000269217.10:c.813C>A	ENSP00000269217.5:p.Ala271=
ENST00000313654.13:c.5640C>A	ENSP00000324532.8:p.Ala1880=
ENST00000399516.7:c.5640C>A	ENSP00000382432.2:p.Ala1880=
ENST00000586709.1:n.28C>A
ENST00000586751.5:c.418C>A
ENST00000587184.5:c.813C>A	ENSP00000466557.1:p.Ala271=
ENST00000588770.5:n.218C>A
NM_000227.4:c.813C>A	NP_000218.3:p.Ala271=
NM_001127717.2:c.5640C>A	NP_001121189.2:p.Ala1880=
NM_001127718.2:c.813C>A	NP_001121190.2:p.Ala271=
NM_198129.2:c.5640C>A	NP_937762.2:p.Ala1880=
XM_011525978.1:c.5667C>A	XP_011524280.1:p.Ala1889=
XM_011525979.1:c.5658C>A	XP_011524281.1:p.Ala1886=
XM_011525980.1:c.5649C>A	XP_011524282.1:p.Ala1883=
XM_011525981.1:c.5535C>A	XP_011524283.1:p.Ala1845=
XM_011525982.1:c.5667C>A	XP_011524284.1:p.Ala1889=
XM_011525978.2:c.5667C>A	XP_011524280.1:p.Ala1889=
XM_011525979.2:c.5658C>A	XP_011524281.1:p.Ala1886=
XM_011525980.2:c.5649C>A	XP_011524282.1:p.Ala1883=
XM_011525981.2:c.5535C>A	XP_011524283.1:p.Ala1845=
XM_011525982.2:c.5667C>A	XP_011524284.1:p.Ala1889=
XM_017025743.1:c.3519C>A	XP_016881232.1:p.Ala1173=
XM_017025744.1:c.1209C>A	XP_016881233.1:p.Ala403=
XR_001753199.1:n.5908C>A
NM_000227.5:c.813C>A	NP_000218.3:p.Ala271=
NM_001127717.3:c.5640C>A	NP_001121189.2:p.Ala1880=
NM_001127718.3:c.813C>A	NP_001121190.2:p.Ala271=
NM_198129.3:c.5640C>A	NP_937762.2:p.Ala1880=
NM_000227.6:c.813C>A MANE Plus Clinical	NP_000218.3:p.Ala271=
NM_001127717.4:c.5640C>A	NP_001121189.2:p.Ala1880=
NM_001127718.4:c.813C>A	NP_001121190.2:p.Ala271=
NM_198129.4:c.5640C>A MANE Select	NP_937762.2:p.Ala1880=