Canonical Allele Identifier: CA402051912

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21530013C>G (hg19) ; chr18:g.23950049C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950049C>G , CM000680.2:g.23950049C>G	GRCh38
NC_000018.9:g.21530013C>G , CM000680.1:g.21530013C>G	GRCh37
NC_000018.8:g.19784011C>G	NCBI36
NG_007853.2:g.265452C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4705C>G MANE Plus Clinical	ENSP00000269217.5:p.Pro1569Ala
ENST00000313654.14:c.9532C>G MANE Select	ENSP00000324532.8:p.Pro3178Ala
ENST00000649721.1:c.6127C>G	ENSP00000497885.1:p.Pro2043Ala
ENST00000269217.10:c.4705C>G	ENSP00000269217.5:p.Pro1569Ala
ENST00000313654.13:c.9532C>G	ENSP00000324532.8:p.Pro3178Ala
ENST00000399516.7:c.9364C>G	ENSP00000382432.2:p.Pro3122Ala
ENST00000587184.5:c.4537C>G	ENSP00000466557.1:p.Pro1513Ala
ENST00000588004.1:c.53C>G
ENST00000588770.5:n.4110C>G
NM_000227.4:c.4705C>G	NP_000218.3:p.Pro1569Ala
NM_001127717.2:c.9364C>G	NP_001121189.2:p.Pro3122Ala
NM_001127718.2:c.4537C>G	NP_001121190.2:p.Pro1513Ala
NM_198129.2:c.9532C>G	NP_937762.2:p.Pro3178Ala
XM_011525978.1:c.9559C>G	XP_011524280.1:p.Pro3187Ala
XM_011525979.1:c.9550C>G	XP_011524281.1:p.Pro3184Ala
XM_011525980.1:c.9541C>G	XP_011524282.1:p.Pro3181Ala
XM_011525981.1:c.9427C>G	XP_011524283.1:p.Pro3143Ala
XM_011525982.1:c.9262C>G	XP_011524284.1:p.Pro3088Ala
XM_011525978.2:c.9559C>G	XP_011524280.1:p.Pro3187Ala
XM_011525979.2:c.9550C>G	XP_011524281.1:p.Pro3184Ala
XM_011525980.2:c.9541C>G	XP_011524282.1:p.Pro3181Ala
XM_011525981.2:c.9427C>G	XP_011524283.1:p.Pro3143Ala
XM_011525982.2:c.9262C>G	XP_011524284.1:p.Pro3088Ala
XM_017025743.1:c.7411C>G	XP_016881232.1:p.Pro2471Ala
XM_017025744.1:c.5101C>G	XP_016881233.1:p.Pro1701Ala
XR_001753199.1:n.9800C>G
NM_000227.5:c.4705C>G	NP_000218.3:p.Pro1569Ala
NM_001127717.3:c.9364C>G	NP_001121189.2:p.Pro3122Ala
NM_001127718.3:c.4537C>G	NP_001121190.2:p.Pro1513Ala
NM_198129.3:c.9532C>G	NP_937762.2:p.Pro3178Ala
NM_000227.6:c.4705C>G MANE Plus Clinical	NP_000218.3:p.Pro1569Ala
NM_001127717.4:c.9364C>G	NP_001121189.2:p.Pro3122Ala
NM_001127718.4:c.4537C>G	NP_001121190.2:p.Pro1513Ala
NM_198129.4:c.9532C>G MANE Select	NP_937762.2:p.Pro3178Ala