Canonical Allele Identifier: CA402064454

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21511031G>C (hg19) ; chr18:g.23931067G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23931067G>C , CM000680.2:g.23931067G>C	GRCh38
NC_000018.9:g.21511031G>C , CM000680.1:g.21511031G>C	GRCh37
NC_000018.8:g.19765029G>C	NCBI36
NG_007853.2:g.246470G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3615G>C MANE Plus Clinical	ENSP00000269217.5:p.Arg1205Ser
ENST00000313654.14:c.8442G>C MANE Select	ENSP00000324532.8:p.Arg2814Ser
ENST00000649721.1:c.5037G>C	ENSP00000497885.1:p.Arg1679Ser
ENST00000269217.10:c.3615G>C	ENSP00000269217.5:p.Arg1205Ser
ENST00000313654.13:c.8442G>C	ENSP00000324532.8:p.Arg2814Ser
ENST00000399516.7:c.8274G>C	ENSP00000382432.2:p.Arg2758Ser
ENST00000586751.5:c.3220G>C
ENST00000587184.5:c.3447G>C	ENSP00000466557.1:p.Arg1149Ser
ENST00000588164.2:c.147G>C	ENSP00000467473.2:p.Arg49Ser
ENST00000588770.5:n.3020G>C
NM_000227.4:c.3615G>C	NP_000218.3:p.Arg1205Ser
NM_001127717.2:c.8274G>C	NP_001121189.2:p.Arg2758Ser
NM_001127718.2:c.3447G>C	NP_001121190.2:p.Arg1149Ser
NM_198129.2:c.8442G>C	NP_937762.2:p.Arg2814Ser
XM_011525978.1:c.8469G>C	XP_011524280.1:p.Arg2823Ser
XM_011525979.1:c.8460G>C	XP_011524281.1:p.Arg2820Ser
XM_011525980.1:c.8451G>C	XP_011524282.1:p.Arg2817Ser
XM_011525981.1:c.8337G>C	XP_011524283.1:p.Arg2779Ser
XM_011525982.1:c.8172G>C	XP_011524284.1:p.Arg2724Ser
XM_011525978.2:c.8469G>C	XP_011524280.1:p.Arg2823Ser
XM_011525979.2:c.8460G>C	XP_011524281.1:p.Arg2820Ser
XM_011525980.2:c.8451G>C	XP_011524282.1:p.Arg2817Ser
XM_011525981.2:c.8337G>C	XP_011524283.1:p.Arg2779Ser
XM_011525982.2:c.8172G>C	XP_011524284.1:p.Arg2724Ser
XM_017025743.1:c.6321G>C	XP_016881232.1:p.Arg2107Ser
XM_017025744.1:c.4011G>C	XP_016881233.1:p.Arg1337Ser
XR_001753199.1:n.8710G>C
NM_000227.5:c.3615G>C	NP_000218.3:p.Arg1205Ser
NM_001127717.3:c.8274G>C	NP_001121189.2:p.Arg2758Ser
NM_001127718.3:c.3447G>C	NP_001121190.2:p.Arg1149Ser
NM_198129.3:c.8442G>C	NP_937762.2:p.Arg2814Ser
NM_000227.6:c.3615G>C MANE Plus Clinical	NP_000218.3:p.Arg1205Ser
NM_001127717.4:c.8274G>C	NP_001121189.2:p.Arg2758Ser
NM_001127718.4:c.3447G>C	NP_001121190.2:p.Arg1149Ser
NM_198129.4:c.8442G>C MANE Select	NP_937762.2:p.Arg2814Ser