Canonical Allele Identifier: CA402059368

Gene: LAMA3

Linked Data

• dbSNP Id: rs1876670881
• gnomAD v3: 18-23915412-C-T
• gnomAD v4: 18-23915412-C-T
• MyVariant Identifiers: chr18:g.21495376C>T (hg19) ; chr18:g.23915412C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915412C>T , CM000680.2:g.23915412C>T	GRCh38
NC_000018.9:g.21495376C>T , CM000680.1:g.21495376C>T	GRCh37
NC_000018.8:g.19749374C>T	NCBI36
NG_007853.2:g.230815C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2941C>T MANE Plus Clinical	ENSP00000269217.5:p.Pro981Ser
ENST00000313654.14:c.7768C>T MANE Select	ENSP00000324532.8:p.Pro2590Ser
ENST00000649721.1:c.4363C>T	ENSP00000497885.1:p.Pro1455Ser
ENST00000269217.10:c.2941C>T	ENSP00000269217.5:p.Pro981Ser
ENST00000313654.13:c.7768C>T	ENSP00000324532.8:p.Pro2590Ser
ENST00000399516.7:c.7600C>T	ENSP00000382432.2:p.Pro2534Ser
ENST00000586751.5:c.2546C>T
ENST00000587184.5:c.2773C>T	ENSP00000466557.1:p.Pro925Ser
ENST00000588770.5:n.2346C>T
NM_000227.4:c.2941C>T	NP_000218.3:p.Pro981Ser
NM_001127717.2:c.7600C>T	NP_001121189.2:p.Pro2534Ser
NM_001127718.2:c.2773C>T	NP_001121190.2:p.Pro925Ser
NM_198129.2:c.7768C>T	NP_937762.2:p.Pro2590Ser
XM_011525978.1:c.7795C>T	XP_011524280.1:p.Pro2599Ser
XM_011525979.1:c.7786C>T	XP_011524281.1:p.Pro2596Ser
XM_011525980.1:c.7777C>T	XP_011524282.1:p.Pro2593Ser
XM_011525981.1:c.7663C>T	XP_011524283.1:p.Pro2555Ser
XM_011525982.1:c.7498C>T	XP_011524284.1:p.Pro2500Ser
XM_011525978.2:c.7795C>T	XP_011524280.1:p.Pro2599Ser
XM_011525979.2:c.7786C>T	XP_011524281.1:p.Pro2596Ser
XM_011525980.2:c.7777C>T	XP_011524282.1:p.Pro2593Ser
XM_011525981.2:c.7663C>T	XP_011524283.1:p.Pro2555Ser
XM_011525982.2:c.7498C>T	XP_011524284.1:p.Pro2500Ser
XM_017025743.1:c.5647C>T	XP_016881232.1:p.Pro1883Ser
XM_017025744.1:c.3337C>T	XP_016881233.1:p.Pro1113Ser
XR_001753199.1:n.8036C>T
NM_000227.5:c.2941C>T	NP_000218.3:p.Pro981Ser
NM_001127717.3:c.7600C>T	NP_001121189.2:p.Pro2534Ser
NM_001127718.3:c.2773C>T	NP_001121190.2:p.Pro925Ser
NM_198129.3:c.7768C>T	NP_937762.2:p.Pro2590Ser
NM_000227.6:c.2941C>T MANE Plus Clinical	NP_000218.3:p.Pro981Ser
NM_001127717.4:c.7600C>T	NP_001121189.2:p.Pro2534Ser
NM_001127718.4:c.2773C>T	NP_001121190.2:p.Pro925Ser
NM_198129.4:c.7768C>T MANE Select	NP_937762.2:p.Pro2590Ser