Canonical Allele Identifier: CA402063254

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508164A>G (hg19) ; chr18:g.23928200A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928200A>G , CM000680.2:g.23928200A>G	GRCh38
NC_000018.9:g.21508164A>G , CM000680.1:g.21508164A>G	GRCh37
NC_000018.8:g.19762162A>G	NCBI36
NG_007853.2:g.243603A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3428A>G MANE Plus Clinical	ENSP00000269217.5:p.Asp1143Gly
ENST00000313654.14:c.8255A>G MANE Select	ENSP00000324532.8:p.Asp2752Gly
ENST00000649721.1:c.4850A>G	ENSP00000497885.1:p.Asp1617Gly
ENST00000269217.10:c.3428A>G	ENSP00000269217.5:p.Asp1143Gly
ENST00000313654.13:c.8255A>G	ENSP00000324532.8:p.Asp2752Gly
ENST00000399516.7:c.8087A>G	ENSP00000382432.2:p.Asp2696Gly
ENST00000586751.5:c.3033A>G
ENST00000587184.5:c.3260A>G	ENSP00000466557.1:p.Asp1087Gly
ENST00000588770.5:n.2833A>G
NM_000227.4:c.3428A>G	NP_000218.3:p.Asp1143Gly
NM_001127717.2:c.8087A>G	NP_001121189.2:p.Asp2696Gly
NM_001127718.2:c.3260A>G	NP_001121190.2:p.Asp1087Gly
NM_198129.2:c.8255A>G	NP_937762.2:p.Asp2752Gly
XM_011525978.1:c.8282A>G	XP_011524280.1:p.Asp2761Gly
XM_011525979.1:c.8273A>G	XP_011524281.1:p.Asp2758Gly
XM_011525980.1:c.8264A>G	XP_011524282.1:p.Asp2755Gly
XM_011525981.1:c.8150A>G	XP_011524283.1:p.Asp2717Gly
XM_011525982.1:c.7985A>G	XP_011524284.1:p.Asp2662Gly
XM_011525978.2:c.8282A>G	XP_011524280.1:p.Asp2761Gly
XM_011525979.2:c.8273A>G	XP_011524281.1:p.Asp2758Gly
XM_011525980.2:c.8264A>G	XP_011524282.1:p.Asp2755Gly
XM_011525981.2:c.8150A>G	XP_011524283.1:p.Asp2717Gly
XM_011525982.2:c.7985A>G	XP_011524284.1:p.Asp2662Gly
XM_017025743.1:c.6134A>G	XP_016881232.1:p.Asp2045Gly
XM_017025744.1:c.3824A>G	XP_016881233.1:p.Asp1275Gly
XR_001753199.1:n.8523A>G
NM_000227.5:c.3428A>G	NP_000218.3:p.Asp1143Gly
NM_001127717.3:c.8087A>G	NP_001121189.2:p.Asp2696Gly
NM_001127718.3:c.3260A>G	NP_001121190.2:p.Asp1087Gly
NM_198129.3:c.8255A>G	NP_937762.2:p.Asp2752Gly
NM_000227.6:c.3428A>G MANE Plus Clinical	NP_000218.3:p.Asp1143Gly
NM_001127717.4:c.8087A>G	NP_001121189.2:p.Asp2696Gly
NM_001127718.4:c.3260A>G	NP_001121190.2:p.Asp1087Gly
NM_198129.4:c.8255A>G MANE Select	NP_937762.2:p.Asp2752Gly