Canonical Allele Identifier: CA402071474

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21444753C>A (hg19) ; chr18:g.23864789C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23864789C>A , CM000680.2:g.23864789C>A	GRCh38
NC_000018.9:g.21444753C>A , CM000680.1:g.21444753C>A	GRCh37
NC_000018.8:g.19698751C>A	NCBI36
NG_007853.2:g.180192C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313654.14:c.4589C>A MANE Select	ENSP00000324532.8:p.Ser1530Tyr
ENST00000649721.1:c.1481C>A	ENSP00000497885.1:p.Ser494Tyr
ENST00000313654.13:c.4589C>A	ENSP00000324532.8:p.Ser1530Tyr
ENST00000399516.7:c.4589C>A	ENSP00000382432.2:p.Ser1530Tyr
NM_001127717.2:c.4589C>A	NP_001121189.2:p.Ser1530Tyr
NM_198129.2:c.4589C>A	NP_937762.2:p.Ser1530Tyr
XM_011525978.1:c.4616C>A	XP_011524280.1:p.Ser1539Tyr
XM_011525979.1:c.4607C>A	XP_011524281.1:p.Ser1536Tyr
XM_011525980.1:c.4598C>A	XP_011524282.1:p.Ser1533Tyr
XM_011525981.1:c.4484C>A	XP_011524283.1:p.Ser1495Tyr
XM_011525982.1:c.4616C>A	XP_011524284.1:p.Ser1539Tyr
XM_011525978.2:c.4616C>A	XP_011524280.1:p.Ser1539Tyr
XM_011525979.2:c.4607C>A	XP_011524281.1:p.Ser1536Tyr
XM_011525980.2:c.4598C>A	XP_011524282.1:p.Ser1533Tyr
XM_011525981.2:c.4484C>A	XP_011524283.1:p.Ser1495Tyr
XM_011525982.2:c.4616C>A	XP_011524284.1:p.Ser1539Tyr
XM_017025743.1:c.2468C>A	XP_016881232.1:p.Ser823Tyr
XM_017025744.1:c.158C>A	XP_016881233.1:p.Ser53Tyr
XR_001753199.1:n.4857C>A
NM_001127717.3:c.4589C>A	NP_001121189.2:p.Ser1530Tyr
NM_198129.3:c.4589C>A	NP_937762.2:p.Ser1530Tyr
NM_001127717.4:c.4589C>A	NP_001121189.2:p.Ser1530Tyr
NM_198129.4:c.4589C>A MANE Select	NP_937762.2:p.Ser1530Tyr