Canonical Allele Identifier: CA503340776

Gene: LAMA3

Linked Data

• COSMIC: COSM1303629 ; COSM1303630
• MyVariant Identifiers: chr18:g.21508633C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928669C>T , CM000680.2:g.23928669C>T	GRCh38
NC_000018.9:g.21508633C>T , CM000680.1:g.21508633C>T	GRCh37
NC_000018.8:g.19762631C>T	NCBI36
NG_007853.2:g.244072C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3513C>T MANE Plus Clinical	ENSP00000269217.5:p.Phe1171=
ENST00000313654.14:c.8340C>T MANE Select	ENSP00000324532.8:p.Phe2780=
ENST00000649721.1:c.4935C>T	ENSP00000497885.1:p.Phe1645=
ENST00000269217.10:c.3513C>T	ENSP00000269217.5:p.Phe1171=
ENST00000313654.13:c.8340C>T	ENSP00000324532.8:p.Phe2780=
ENST00000399516.7:c.8172C>T	ENSP00000382432.2:p.Phe2724=
ENST00000586751.5:c.3118C>T
ENST00000587184.5:c.3345C>T	ENSP00000466557.1:p.Phe1115=
ENST00000588164.2:c.45C>T	ENSP00000467473.2:p.Phe15=
ENST00000588770.5:n.2918C>T
NM_000227.4:c.3513C>T	NP_000218.3:p.Phe1171=
NM_001127717.2:c.8172C>T	NP_001121189.2:p.Phe2724=
NM_001127718.2:c.3345C>T	NP_001121190.2:p.Phe1115=
NM_198129.2:c.8340C>T	NP_937762.2:p.Phe2780=
XM_011525978.1:c.8367C>T	XP_011524280.1:p.Phe2789=
XM_011525979.1:c.8358C>T	XP_011524281.1:p.Phe2786=
XM_011525980.1:c.8349C>T	XP_011524282.1:p.Phe2783=
XM_011525981.1:c.8235C>T	XP_011524283.1:p.Phe2745=
XM_011525982.1:c.8070C>T	XP_011524284.1:p.Phe2690=
XM_011525978.2:c.8367C>T	XP_011524280.1:p.Phe2789=
XM_011525979.2:c.8358C>T	XP_011524281.1:p.Phe2786=
XM_011525980.2:c.8349C>T	XP_011524282.1:p.Phe2783=
XM_011525981.2:c.8235C>T	XP_011524283.1:p.Phe2745=
XM_011525982.2:c.8070C>T	XP_011524284.1:p.Phe2690=
XM_017025743.1:c.6219C>T	XP_016881232.1:p.Phe2073=
XM_017025744.1:c.3909C>T	XP_016881233.1:p.Phe1303=
XR_001753199.1:n.8608C>T
NM_000227.5:c.3513C>T	NP_000218.3:p.Phe1171=
NM_001127717.3:c.8172C>T	NP_001121189.2:p.Phe2724=
NM_001127718.3:c.3345C>T	NP_001121190.2:p.Phe1115=
NM_198129.3:c.8340C>T	NP_937762.2:p.Phe2780=
NM_000227.6:c.3513C>T MANE Plus Clinical	NP_000218.3:p.Phe1171=
NM_001127717.4:c.8172C>T	NP_001121189.2:p.Phe2724=
NM_001127718.4:c.3345C>T	NP_001121190.2:p.Phe1115=
NM_198129.4:c.8340C>T MANE Select	NP_937762.2:p.Phe2780=