Canonical Allele Identifier: CA402051775

Gene: LAMA3

Linked Data

• dbSNP Id: rs2082844071
• gnomAD v3: 18-23949885-G-C
• gnomAD v4: 18-23949885-G-C
• MyVariant Identifiers: chr18:g.21529849G>C (hg19) ; chr18:g.23949885G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23949885G>C , CM000680.2:g.23949885G>C	GRCh38
NC_000018.9:g.21529849G>C , CM000680.1:g.21529849G>C	GRCh37
NC_000018.8:g.19783847G>C	NCBI36
NG_007853.2:g.265288G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4645G>C MANE Plus Clinical	ENSP00000269217.5:p.Gly1549Arg
ENST00000313654.14:c.9472G>C MANE Select	ENSP00000324532.8:p.Gly3158Arg
ENST00000649721.1:c.6067G>C	ENSP00000497885.1:p.Gly2023Arg
ENST00000269217.10:c.4645G>C	ENSP00000269217.5:p.Gly1549Arg
ENST00000313654.13:c.9472G>C	ENSP00000324532.8:p.Gly3158Arg
ENST00000399516.7:c.9304G>C	ENSP00000382432.2:p.Gly3102Arg
ENST00000587184.5:c.4477G>C	ENSP00000466557.1:p.Gly1493Arg
ENST00000588770.5:n.4050G>C
NM_000227.4:c.4645G>C	NP_000218.3:p.Gly1549Arg
NM_001127717.2:c.9304G>C	NP_001121189.2:p.Gly3102Arg
NM_001127718.2:c.4477G>C	NP_001121190.2:p.Gly1493Arg
NM_198129.2:c.9472G>C	NP_937762.2:p.Gly3158Arg
XM_011525978.1:c.9499G>C	XP_011524280.1:p.Gly3167Arg
XM_011525979.1:c.9490G>C	XP_011524281.1:p.Gly3164Arg
XM_011525980.1:c.9481G>C	XP_011524282.1:p.Gly3161Arg
XM_011525981.1:c.9367G>C	XP_011524283.1:p.Gly3123Arg
XM_011525982.1:c.9202G>C	XP_011524284.1:p.Gly3068Arg
XM_011525978.2:c.9499G>C	XP_011524280.1:p.Gly3167Arg
XM_011525979.2:c.9490G>C	XP_011524281.1:p.Gly3164Arg
XM_011525980.2:c.9481G>C	XP_011524282.1:p.Gly3161Arg
XM_011525981.2:c.9367G>C	XP_011524283.1:p.Gly3123Arg
XM_011525982.2:c.9202G>C	XP_011524284.1:p.Gly3068Arg
XM_017025743.1:c.7351G>C	XP_016881232.1:p.Gly2451Arg
XM_017025744.1:c.5041G>C	XP_016881233.1:p.Gly1681Arg
XR_001753199.1:n.9740G>C
NM_000227.5:c.4645G>C	NP_000218.3:p.Gly1549Arg
NM_001127717.3:c.9304G>C	NP_001121189.2:p.Gly3102Arg
NM_001127718.3:c.4477G>C	NP_001121190.2:p.Gly1493Arg
NM_198129.3:c.9472G>C	NP_937762.2:p.Gly3158Arg
NM_000227.6:c.4645G>C MANE Plus Clinical	NP_000218.3:p.Gly1549Arg
NM_001127717.4:c.9304G>C	NP_001121189.2:p.Gly3102Arg
NM_001127718.4:c.4477G>C	NP_001121190.2:p.Gly1493Arg
NM_198129.4:c.9472G>C MANE Select	NP_937762.2:p.Gly3158Arg