Canonical Allele Identifier: CA503334768

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21483023A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903059A>T , CM000680.2:g.23903059A>T	GRCh38
NC_000018.9:g.21483023A>T , CM000680.1:g.21483023A>T	GRCh37
NC_000018.8:g.19737021A>T	NCBI36
NG_007853.2:g.218462A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1425A>T MANE Plus Clinical	ENSP00000269217.5:p.Leu475=
ENST00000313654.14:c.6252A>T MANE Select	ENSP00000324532.8:p.Leu2084=
ENST00000649721.1:c.3144A>T	ENSP00000497885.1:p.Leu1048=
ENST00000269217.10:c.1425A>T	ENSP00000269217.5:p.Leu475=
ENST00000313654.13:c.6252A>T	ENSP00000324532.8:p.Leu2084=
ENST00000399516.7:c.6084A>T	ENSP00000382432.2:p.Leu2028=
ENST00000586751.5:c.1030A>T
ENST00000587184.5:c.1257A>T	ENSP00000466557.1:p.Leu419=
ENST00000588770.5:n.830A>T
NM_000227.4:c.1425A>T	NP_000218.3:p.Leu475=
NM_001127717.2:c.6084A>T	NP_001121189.2:p.Leu2028=
NM_001127718.2:c.1257A>T	NP_001121190.2:p.Leu419=
NM_198129.2:c.6252A>T	NP_937762.2:p.Leu2084=
XM_011525978.1:c.6279A>T	XP_011524280.1:p.Leu2093=
XM_011525979.1:c.6270A>T	XP_011524281.1:p.Leu2090=
XM_011525980.1:c.6261A>T	XP_011524282.1:p.Leu2087=
XM_011525981.1:c.6147A>T	XP_011524283.1:p.Leu2049=
XM_011525982.1:c.6279A>T	XP_011524284.1:p.Leu2093=
XM_011525978.2:c.6279A>T	XP_011524280.1:p.Leu2093=
XM_011525979.2:c.6270A>T	XP_011524281.1:p.Leu2090=
XM_011525980.2:c.6261A>T	XP_011524282.1:p.Leu2087=
XM_011525981.2:c.6147A>T	XP_011524283.1:p.Leu2049=
XM_011525982.2:c.6279A>T	XP_011524284.1:p.Leu2093=
XM_017025743.1:c.4131A>T	XP_016881232.1:p.Leu1377=
XM_017025744.1:c.1821A>T	XP_016881233.1:p.Leu607=
XR_001753199.1:n.6520A>T
NM_000227.5:c.1425A>T	NP_000218.3:p.Leu475=
NM_001127717.3:c.6084A>T	NP_001121189.2:p.Leu2028=
NM_001127718.3:c.1257A>T	NP_001121190.2:p.Leu419=
NM_198129.3:c.6252A>T	NP_937762.2:p.Leu2084=
NM_000227.6:c.1425A>T MANE Plus Clinical	NP_000218.3:p.Leu475=
NM_001127717.4:c.6084A>T	NP_001121189.2:p.Leu2028=
NM_001127718.4:c.1257A>T	NP_001121190.2:p.Leu419=
NM_198129.4:c.6252A>T MANE Select	NP_937762.2:p.Leu2084=