Canonical Allele Identifier: CA402064715

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21511092C>A (hg19) ; chr18:g.23931128C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23931128C>A , CM000680.2:g.23931128C>A	GRCh38
NC_000018.9:g.21511092C>A , CM000680.1:g.21511092C>A	GRCh37
NC_000018.8:g.19765090C>A	NCBI36
NG_007853.2:g.246531C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3676C>A MANE Plus Clinical	ENSP00000269217.5:p.Pro1226Thr
ENST00000313654.14:c.8503C>A MANE Select	ENSP00000324532.8:p.Pro2835Thr
ENST00000649721.1:c.5098C>A	ENSP00000497885.1:p.Pro1700Thr
ENST00000269217.10:c.3676C>A	ENSP00000269217.5:p.Pro1226Thr
ENST00000313654.13:c.8503C>A	ENSP00000324532.8:p.Pro2835Thr
ENST00000399516.7:c.8335C>A	ENSP00000382432.2:p.Pro2779Thr
ENST00000586751.5:c.3281C>A
ENST00000587184.5:c.3508C>A	ENSP00000466557.1:p.Pro1170Thr
ENST00000588164.2:c.208C>A	ENSP00000467473.2:p.Pro70Thr
ENST00000588770.5:n.3081C>A
NM_000227.4:c.3676C>A	NP_000218.3:p.Pro1226Thr
NM_001127717.2:c.8335C>A	NP_001121189.2:p.Pro2779Thr
NM_001127718.2:c.3508C>A	NP_001121190.2:p.Pro1170Thr
NM_198129.2:c.8503C>A	NP_937762.2:p.Pro2835Thr
XM_011525978.1:c.8530C>A	XP_011524280.1:p.Pro2844Thr
XM_011525979.1:c.8521C>A	XP_011524281.1:p.Pro2841Thr
XM_011525980.1:c.8512C>A	XP_011524282.1:p.Pro2838Thr
XM_011525981.1:c.8398C>A	XP_011524283.1:p.Pro2800Thr
XM_011525982.1:c.8233C>A	XP_011524284.1:p.Pro2745Thr
XM_011525978.2:c.8530C>A	XP_011524280.1:p.Pro2844Thr
XM_011525979.2:c.8521C>A	XP_011524281.1:p.Pro2841Thr
XM_011525980.2:c.8512C>A	XP_011524282.1:p.Pro2838Thr
XM_011525981.2:c.8398C>A	XP_011524283.1:p.Pro2800Thr
XM_011525982.2:c.8233C>A	XP_011524284.1:p.Pro2745Thr
XM_017025743.1:c.6382C>A	XP_016881232.1:p.Pro2128Thr
XM_017025744.1:c.4072C>A	XP_016881233.1:p.Pro1358Thr
XR_001753199.1:n.8771C>A
NM_000227.5:c.3676C>A	NP_000218.3:p.Pro1226Thr
NM_001127717.3:c.8335C>A	NP_001121189.2:p.Pro2779Thr
NM_001127718.3:c.3508C>A	NP_001121190.2:p.Pro1170Thr
NM_198129.3:c.8503C>A	NP_937762.2:p.Pro2835Thr
NM_000227.6:c.3676C>A MANE Plus Clinical	NP_000218.3:p.Pro1226Thr
NM_001127717.4:c.8335C>A	NP_001121189.2:p.Pro2779Thr
NM_001127718.4:c.3508C>A	NP_001121190.2:p.Pro1170Thr
NM_198129.4:c.8503C>A MANE Select	NP_937762.2:p.Pro2835Thr