Canonical Allele Identifier: CA402071509

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21444762G>T (hg19) ; chr18:g.23864798G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23864798G>T , CM000680.2:g.23864798G>T	GRCh38
NC_000018.9:g.21444762G>T , CM000680.1:g.21444762G>T	GRCh37
NC_000018.8:g.19698760G>T	NCBI36
NG_007853.2:g.180201G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313654.14:c.4598G>T MANE Select	ENSP00000324532.8:p.Gly1533Val
ENST00000649721.1:c.1490G>T	ENSP00000497885.1:p.Gly497Val
ENST00000313654.13:c.4598G>T	ENSP00000324532.8:p.Gly1533Val
ENST00000399516.7:c.4598G>T	ENSP00000382432.2:p.Gly1533Val
NM_001127717.2:c.4598G>T	NP_001121189.2:p.Gly1533Val
NM_198129.2:c.4598G>T	NP_937762.2:p.Gly1533Val
XM_011525978.1:c.4625G>T	XP_011524280.1:p.Gly1542Val
XM_011525979.1:c.4616G>T	XP_011524281.1:p.Gly1539Val
XM_011525980.1:c.4607G>T	XP_011524282.1:p.Gly1536Val
XM_011525981.1:c.4493G>T	XP_011524283.1:p.Gly1498Val
XM_011525982.1:c.4625G>T	XP_011524284.1:p.Gly1542Val
XM_011525978.2:c.4625G>T	XP_011524280.1:p.Gly1542Val
XM_011525979.2:c.4616G>T	XP_011524281.1:p.Gly1539Val
XM_011525980.2:c.4607G>T	XP_011524282.1:p.Gly1536Val
XM_011525981.2:c.4493G>T	XP_011524283.1:p.Gly1498Val
XM_011525982.2:c.4625G>T	XP_011524284.1:p.Gly1542Val
XM_017025743.1:c.2477G>T	XP_016881232.1:p.Gly826Val
XM_017025744.1:c.167G>T	XP_016881233.1:p.Gly56Val
XR_001753199.1:n.4866G>T
NM_001127717.3:c.4598G>T	NP_001121189.2:p.Gly1533Val
NM_198129.3:c.4598G>T	NP_937762.2:p.Gly1533Val
NM_001127717.4:c.4598G>T	NP_001121189.2:p.Gly1533Val
NM_198129.4:c.4598G>T MANE Select	NP_937762.2:p.Gly1533Val