Canonical Allele Identifier: CA503340677

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508198C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928234C>T , CM000680.2:g.23928234C>T	GRCh38
NC_000018.9:g.21508198C>T , CM000680.1:g.21508198C>T	GRCh37
NC_000018.8:g.19762196C>T	NCBI36
NG_007853.2:g.243637C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3462C>T MANE Plus Clinical	ENSP00000269217.5:p.Asp1154=
ENST00000313654.14:c.8289C>T MANE Select	ENSP00000324532.8:p.Asp2763=
ENST00000649721.1:c.4884C>T	ENSP00000497885.1:p.Asp1628=
ENST00000269217.10:c.3462C>T	ENSP00000269217.5:p.Asp1154=
ENST00000313654.13:c.8289C>T	ENSP00000324532.8:p.Asp2763=
ENST00000399516.7:c.8121C>T	ENSP00000382432.2:p.Asp2707=
ENST00000586751.5:c.3067C>T
ENST00000587184.5:c.3294C>T	ENSP00000466557.1:p.Asp1098=
ENST00000588770.5:n.2867C>T
NM_000227.4:c.3462C>T	NP_000218.3:p.Asp1154=
NM_001127717.2:c.8121C>T	NP_001121189.2:p.Asp2707=
NM_001127718.2:c.3294C>T	NP_001121190.2:p.Asp1098=
NM_198129.2:c.8289C>T	NP_937762.2:p.Asp2763=
XM_011525978.1:c.8316C>T	XP_011524280.1:p.Asp2772=
XM_011525979.1:c.8307C>T	XP_011524281.1:p.Asp2769=
XM_011525980.1:c.8298C>T	XP_011524282.1:p.Asp2766=
XM_011525981.1:c.8184C>T	XP_011524283.1:p.Asp2728=
XM_011525982.1:c.8019C>T	XP_011524284.1:p.Asp2673=
XM_011525978.2:c.8316C>T	XP_011524280.1:p.Asp2772=
XM_011525979.2:c.8307C>T	XP_011524281.1:p.Asp2769=
XM_011525980.2:c.8298C>T	XP_011524282.1:p.Asp2766=
XM_011525981.2:c.8184C>T	XP_011524283.1:p.Asp2728=
XM_011525982.2:c.8019C>T	XP_011524284.1:p.Asp2673=
XM_017025743.1:c.6168C>T	XP_016881232.1:p.Asp2056=
XM_017025744.1:c.3858C>T	XP_016881233.1:p.Asp1286=
XR_001753199.1:n.8557C>T
NM_000227.5:c.3462C>T	NP_000218.3:p.Asp1154=
NM_001127717.3:c.8121C>T	NP_001121189.2:p.Asp2707=
NM_001127718.3:c.3294C>T	NP_001121190.2:p.Asp1098=
NM_198129.3:c.8289C>T	NP_937762.2:p.Asp2763=
NM_000227.6:c.3462C>T MANE Plus Clinical	NP_000218.3:p.Asp1154=
NM_001127717.4:c.8121C>T	NP_001121189.2:p.Asp2707=
NM_001127718.4:c.3294C>T	NP_001121190.2:p.Asp1098=
NM_198129.4:c.8289C>T MANE Select	NP_937762.2:p.Asp2763=