Canonical Allele Identifier: CA402063397

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23928227-C-A
• MyVariant Identifiers: chr18:g.21508191C>A (hg19) ; chr18:g.23928227C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928227C>A , CM000680.2:g.23928227C>A	GRCh38
NC_000018.9:g.21508191C>A , CM000680.1:g.21508191C>A	GRCh37
NC_000018.8:g.19762189C>A	NCBI36
NG_007853.2:g.243630C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3455C>A MANE Plus Clinical	ENSP00000269217.5:p.Ser1152Ter
ENST00000313654.14:c.8282C>A MANE Select	ENSP00000324532.8:p.Ser2761Ter
ENST00000649721.1:c.4877C>A	ENSP00000497885.1:p.Ser1626Ter
ENST00000269217.10:c.3455C>A	ENSP00000269217.5:p.Ser1152Ter
ENST00000313654.13:c.8282C>A	ENSP00000324532.8:p.Ser2761Ter
ENST00000399516.7:c.8114C>A	ENSP00000382432.2:p.Ser2705Ter
ENST00000586751.5:c.3060C>A
ENST00000587184.5:c.3287C>A	ENSP00000466557.1:p.Ser1096Ter
ENST00000588770.5:n.2860C>A
NM_000227.4:c.3455C>A	NP_000218.3:p.Ser1152Ter
NM_001127717.2:c.8114C>A	NP_001121189.2:p.Ser2705Ter
NM_001127718.2:c.3287C>A	NP_001121190.2:p.Ser1096Ter
NM_198129.2:c.8282C>A	NP_937762.2:p.Ser2761Ter
XM_011525978.1:c.8309C>A	XP_011524280.1:p.Ser2770Ter
XM_011525979.1:c.8300C>A	XP_011524281.1:p.Ser2767Ter
XM_011525980.1:c.8291C>A	XP_011524282.1:p.Ser2764Ter
XM_011525981.1:c.8177C>A	XP_011524283.1:p.Ser2726Ter
XM_011525982.1:c.8012C>A	XP_011524284.1:p.Ser2671Ter
XM_011525978.2:c.8309C>A	XP_011524280.1:p.Ser2770Ter
XM_011525979.2:c.8300C>A	XP_011524281.1:p.Ser2767Ter
XM_011525980.2:c.8291C>A	XP_011524282.1:p.Ser2764Ter
XM_011525981.2:c.8177C>A	XP_011524283.1:p.Ser2726Ter
XM_011525982.2:c.8012C>A	XP_011524284.1:p.Ser2671Ter
XM_017025743.1:c.6161C>A	XP_016881232.1:p.Ser2054Ter
XM_017025744.1:c.3851C>A	XP_016881233.1:p.Ser1284Ter
XR_001753199.1:n.8550C>A
NM_000227.5:c.3455C>A	NP_000218.3:p.Ser1152Ter
NM_001127717.3:c.8114C>A	NP_001121189.2:p.Ser2705Ter
NM_001127718.3:c.3287C>A	NP_001121190.2:p.Ser1096Ter
NM_198129.3:c.8282C>A	NP_937762.2:p.Ser2761Ter
NM_000227.6:c.3455C>A MANE Plus Clinical	NP_000218.3:p.Ser1152Ter
NM_001127717.4:c.8114C>A	NP_001121189.2:p.Ser2705Ter
NM_001127718.4:c.3287C>A	NP_001121190.2:p.Ser1096Ter
NM_198129.4:c.8282C>A MANE Select	NP_937762.2:p.Ser2761Ter