Canonical Allele Identifier: CA402063282

Gene: LAMA3

Linked Data

• ClinVar Variation Id: 2850481
• ClinVar RCV Id: RCV003688312
• MyVariant Identifiers: chr18:g.21508172G>T (hg19) ; chr18:g.23928208G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928208G>T , CM000680.2:g.23928208G>T	GRCh38
NC_000018.9:g.21508172G>T , CM000680.1:g.21508172G>T	GRCh37
NC_000018.8:g.19762170G>T	NCBI36
NG_007853.2:g.243611G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3436G>T MANE Plus Clinical	ENSP00000269217.5:p.Gly1146Ter
ENST00000313654.14:c.8263G>T MANE Select	ENSP00000324532.8:p.Gly2755Ter
ENST00000649721.1:c.4858G>T	ENSP00000497885.1:p.Gly1620Ter
ENST00000269217.10:c.3436G>T	ENSP00000269217.5:p.Gly1146Ter
ENST00000313654.13:c.8263G>T	ENSP00000324532.8:p.Gly2755Ter
ENST00000399516.7:c.8095G>T	ENSP00000382432.2:p.Gly2699Ter
ENST00000586751.5:c.3041G>T
ENST00000587184.5:c.3268G>T	ENSP00000466557.1:p.Gly1090Ter
ENST00000588770.5:n.2841G>T
NM_000227.4:c.3436G>T	NP_000218.3:p.Gly1146Ter
NM_001127717.2:c.8095G>T	NP_001121189.2:p.Gly2699Ter
NM_001127718.2:c.3268G>T	NP_001121190.2:p.Gly1090Ter
NM_198129.2:c.8263G>T	NP_937762.2:p.Gly2755Ter
XM_011525978.1:c.8290G>T	XP_011524280.1:p.Gly2764Ter
XM_011525979.1:c.8281G>T	XP_011524281.1:p.Gly2761Ter
XM_011525980.1:c.8272G>T	XP_011524282.1:p.Gly2758Ter
XM_011525981.1:c.8158G>T	XP_011524283.1:p.Gly2720Ter
XM_011525982.1:c.7993G>T	XP_011524284.1:p.Gly2665Ter
XM_011525978.2:c.8290G>T	XP_011524280.1:p.Gly2764Ter
XM_011525979.2:c.8281G>T	XP_011524281.1:p.Gly2761Ter
XM_011525980.2:c.8272G>T	XP_011524282.1:p.Gly2758Ter
XM_011525981.2:c.8158G>T	XP_011524283.1:p.Gly2720Ter
XM_011525982.2:c.7993G>T	XP_011524284.1:p.Gly2665Ter
XM_017025743.1:c.6142G>T	XP_016881232.1:p.Gly2048Ter
XM_017025744.1:c.3832G>T	XP_016881233.1:p.Gly1278Ter
XR_001753199.1:n.8531G>T
NM_000227.5:c.3436G>T	NP_000218.3:p.Gly1146Ter
NM_001127717.3:c.8095G>T	NP_001121189.2:p.Gly2699Ter
NM_001127718.3:c.3268G>T	NP_001121190.2:p.Gly1090Ter
NM_198129.3:c.8263G>T	NP_937762.2:p.Gly2755Ter
NM_000227.6:c.3436G>T MANE Plus Clinical	NP_000218.3:p.Gly1146Ter
NM_001127717.4:c.8095G>T	NP_001121189.2:p.Gly2699Ter
NM_001127718.4:c.3268G>T	NP_001121190.2:p.Gly1090Ter
NM_198129.4:c.8263G>T MANE Select	NP_937762.2:p.Gly2755Ter