Canonical Allele Identifier: CA402051998

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21530052C>A (hg19) ; chr18:g.23950088C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950088C>A , CM000680.2:g.23950088C>A	GRCh38
NC_000018.9:g.21530052C>A , CM000680.1:g.21530052C>A	GRCh37
NC_000018.8:g.19784050C>A	NCBI36
NG_007853.2:g.265491C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4744C>A MANE Plus Clinical	ENSP00000269217.5:p.Leu1582Ile
ENST00000313654.14:c.9571C>A MANE Select	ENSP00000324532.8:p.Leu3191Ile
ENST00000649721.1:c.6166C>A	ENSP00000497885.1:p.Leu2056Ile
ENST00000269217.10:c.4744C>A	ENSP00000269217.5:p.Leu1582Ile
ENST00000313654.13:c.9571C>A	ENSP00000324532.8:p.Leu3191Ile
ENST00000399516.7:c.9403C>A	ENSP00000382432.2:p.Leu3135Ile
ENST00000587184.5:c.4576C>A	ENSP00000466557.1:p.Leu1526Ile
ENST00000588004.1:c.92C>A
ENST00000588770.5:n.4149C>A
NM_000227.4:c.4744C>A	NP_000218.3:p.Leu1582Ile
NM_001127717.2:c.9403C>A	NP_001121189.2:p.Leu3135Ile
NM_001127718.2:c.4576C>A	NP_001121190.2:p.Leu1526Ile
NM_198129.2:c.9571C>A	NP_937762.2:p.Leu3191Ile
XM_011525978.1:c.9598C>A	XP_011524280.1:p.Leu3200Ile
XM_011525979.1:c.9589C>A	XP_011524281.1:p.Leu3197Ile
XM_011525980.1:c.9580C>A	XP_011524282.1:p.Leu3194Ile
XM_011525981.1:c.9466C>A	XP_011524283.1:p.Leu3156Ile
XM_011525982.1:c.9301C>A	XP_011524284.1:p.Leu3101Ile
XM_011525978.2:c.9598C>A	XP_011524280.1:p.Leu3200Ile
XM_011525979.2:c.9589C>A	XP_011524281.1:p.Leu3197Ile
XM_011525980.2:c.9580C>A	XP_011524282.1:p.Leu3194Ile
XM_011525981.2:c.9466C>A	XP_011524283.1:p.Leu3156Ile
XM_011525982.2:c.9301C>A	XP_011524284.1:p.Leu3101Ile
XM_017025743.1:c.7450C>A	XP_016881232.1:p.Leu2484Ile
XM_017025744.1:c.5140C>A	XP_016881233.1:p.Leu1714Ile
XR_001753199.1:n.9839C>A
NM_000227.5:c.4744C>A	NP_000218.3:p.Leu1582Ile
NM_001127717.3:c.9403C>A	NP_001121189.2:p.Leu3135Ile
NM_001127718.3:c.4576C>A	NP_001121190.2:p.Leu1526Ile
NM_198129.3:c.9571C>A	NP_937762.2:p.Leu3191Ile
NM_000227.6:c.4744C>A MANE Plus Clinical	NP_000218.3:p.Leu1582Ile
NM_001127717.4:c.9403C>A	NP_001121189.2:p.Leu3135Ile
NM_001127718.4:c.4576C>A	NP_001121190.2:p.Leu1526Ile
NM_198129.4:c.9571C>A MANE Select	NP_937762.2:p.Leu3191Ile