Canonical Allele Identifier: CA402051454

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21485568C>A (hg19) ; chr18:g.23905604C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905604C>A , CM000680.2:g.23905604C>A	GRCh38
NC_000018.9:g.21485568C>A , CM000680.1:g.21485568C>A	GRCh37
NC_000018.8:g.19739566C>A	NCBI36
NG_007853.2:g.221007C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1871C>A MANE Plus Clinical	ENSP00000269217.5:p.Thr624Lys
ENST00000313654.14:c.6698C>A MANE Select	ENSP00000324532.8:p.Thr2233Lys
ENST00000649721.1:c.3590C>A	ENSP00000497885.1:p.Thr1197Lys
ENST00000269217.10:c.1871C>A	ENSP00000269217.5:p.Thr624Lys
ENST00000313654.13:c.6698C>A	ENSP00000324532.8:p.Thr2233Lys
ENST00000399516.7:c.6530C>A	ENSP00000382432.2:p.Thr2177Lys
ENST00000586751.5:c.1476C>A
ENST00000587184.5:c.1703C>A	ENSP00000466557.1:p.Thr568Lys
ENST00000588770.5:n.1276C>A
NM_000227.4:c.1871C>A	NP_000218.3:p.Thr624Lys
NM_001127717.2:c.6530C>A	NP_001121189.2:p.Thr2177Lys
NM_001127718.2:c.1703C>A	NP_001121190.2:p.Thr568Lys
NM_198129.2:c.6698C>A	NP_937762.2:p.Thr2233Lys
XM_011525978.1:c.6725C>A	XP_011524280.1:p.Thr2242Lys
XM_011525979.1:c.6716C>A	XP_011524281.1:p.Thr2239Lys
XM_011525980.1:c.6707C>A	XP_011524282.1:p.Thr2236Lys
XM_011525981.1:c.6593C>A	XP_011524283.1:p.Thr2198Lys
XM_011525982.1:c.6725C>A	XP_011524284.1:p.Thr2242Lys
XM_011525978.2:c.6725C>A	XP_011524280.1:p.Thr2242Lys
XM_011525979.2:c.6716C>A	XP_011524281.1:p.Thr2239Lys
XM_011525980.2:c.6707C>A	XP_011524282.1:p.Thr2236Lys
XM_011525981.2:c.6593C>A	XP_011524283.1:p.Thr2198Lys
XM_011525982.2:c.6725C>A	XP_011524284.1:p.Thr2242Lys
XM_017025743.1:c.4577C>A	XP_016881232.1:p.Thr1526Lys
XM_017025744.1:c.2267C>A	XP_016881233.1:p.Thr756Lys
XR_001753199.1:n.6966C>A
NM_000227.5:c.1871C>A	NP_000218.3:p.Thr624Lys
NM_001127717.3:c.6530C>A	NP_001121189.2:p.Thr2177Lys
NM_001127718.3:c.1703C>A	NP_001121190.2:p.Thr568Lys
NM_198129.3:c.6698C>A	NP_937762.2:p.Thr2233Lys
NM_000227.6:c.1871C>A MANE Plus Clinical	NP_000218.3:p.Thr624Lys
NM_001127717.4:c.6530C>A	NP_001121189.2:p.Thr2177Lys
NM_001127718.4:c.1703C>A	NP_001121190.2:p.Thr568Lys
NM_198129.4:c.6698C>A MANE Select	NP_937762.2:p.Thr2233Lys