Canonical Allele Identifier: CA503341174

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23931130-A-G
• MyVariant Identifiers: chr18:g.21511094A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23931130A>G , CM000680.2:g.23931130A>G	GRCh38
NC_000018.9:g.21511094A>G , CM000680.1:g.21511094A>G	GRCh37
NC_000018.8:g.19765092A>G	NCBI36
NG_007853.2:g.246533A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3678A>G MANE Plus Clinical	ENSP00000269217.5:p.Pro1226=
ENST00000313654.14:c.8505A>G MANE Select	ENSP00000324532.8:p.Pro2835=
ENST00000649721.1:c.5100A>G	ENSP00000497885.1:p.Pro1700=
ENST00000269217.10:c.3678A>G	ENSP00000269217.5:p.Pro1226=
ENST00000313654.13:c.8505A>G	ENSP00000324532.8:p.Pro2835=
ENST00000399516.7:c.8337A>G	ENSP00000382432.2:p.Pro2779=
ENST00000586751.5:c.3283A>G
ENST00000587184.5:c.3510A>G	ENSP00000466557.1:p.Pro1170=
ENST00000588164.2:c.210A>G	ENSP00000467473.2:p.Pro70=
ENST00000588770.5:n.3083A>G
NM_000227.4:c.3678A>G	NP_000218.3:p.Pro1226=
NM_001127717.2:c.8337A>G	NP_001121189.2:p.Pro2779=
NM_001127718.2:c.3510A>G	NP_001121190.2:p.Pro1170=
NM_198129.2:c.8505A>G	NP_937762.2:p.Pro2835=
XM_011525978.1:c.8532A>G	XP_011524280.1:p.Pro2844=
XM_011525979.1:c.8523A>G	XP_011524281.1:p.Pro2841=
XM_011525980.1:c.8514A>G	XP_011524282.1:p.Pro2838=
XM_011525981.1:c.8400A>G	XP_011524283.1:p.Pro2800=
XM_011525982.1:c.8235A>G	XP_011524284.1:p.Pro2745=
XM_011525978.2:c.8532A>G	XP_011524280.1:p.Pro2844=
XM_011525979.2:c.8523A>G	XP_011524281.1:p.Pro2841=
XM_011525980.2:c.8514A>G	XP_011524282.1:p.Pro2838=
XM_011525981.2:c.8400A>G	XP_011524283.1:p.Pro2800=
XM_011525982.2:c.8235A>G	XP_011524284.1:p.Pro2745=
XM_017025743.1:c.6384A>G	XP_016881232.1:p.Pro2128=
XM_017025744.1:c.4074A>G	XP_016881233.1:p.Pro1358=
XR_001753199.1:n.8773A>G
NM_000227.5:c.3678A>G	NP_000218.3:p.Pro1226=
NM_001127717.3:c.8337A>G	NP_001121189.2:p.Pro2779=
NM_001127718.3:c.3510A>G	NP_001121190.2:p.Pro1170=
NM_198129.3:c.8505A>G	NP_937762.2:p.Pro2835=
NM_000227.6:c.3678A>G MANE Plus Clinical	NP_000218.3:p.Pro1226=
NM_001127717.4:c.8337A>G	NP_001121189.2:p.Pro2779=
NM_001127718.4:c.3510A>G	NP_001121190.2:p.Pro1170=
NM_198129.4:c.8505A>G MANE Select	NP_937762.2:p.Pro2835=