Canonical Allele Identifier: CA503340635

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508141C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928177C>G , CM000680.2:g.23928177C>G	GRCh38
NC_000018.9:g.21508141C>G , CM000680.1:g.21508141C>G	GRCh37
NC_000018.8:g.19762139C>G	NCBI36
NG_007853.2:g.243580C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3405C>G MANE Plus Clinical	ENSP00000269217.5:p.Thr1135=
ENST00000313654.14:c.8232C>G MANE Select	ENSP00000324532.8:p.Thr2744=
ENST00000649721.1:c.4827C>G	ENSP00000497885.1:p.Thr1609=
ENST00000269217.10:c.3405C>G	ENSP00000269217.5:p.Thr1135=
ENST00000313654.13:c.8232C>G	ENSP00000324532.8:p.Thr2744=
ENST00000399516.7:c.8064C>G	ENSP00000382432.2:p.Thr2688=
ENST00000586751.5:c.3010C>G
ENST00000587184.5:c.3237C>G	ENSP00000466557.1:p.Thr1079=
ENST00000588770.5:n.2810C>G
NM_000227.4:c.3405C>G	NP_000218.3:p.Thr1135=
NM_001127717.2:c.8064C>G	NP_001121189.2:p.Thr2688=
NM_001127718.2:c.3237C>G	NP_001121190.2:p.Thr1079=
NM_198129.2:c.8232C>G	NP_937762.2:p.Thr2744=
XM_011525978.1:c.8259C>G	XP_011524280.1:p.Thr2753=
XM_011525979.1:c.8250C>G	XP_011524281.1:p.Thr2750=
XM_011525980.1:c.8241C>G	XP_011524282.1:p.Thr2747=
XM_011525981.1:c.8127C>G	XP_011524283.1:p.Thr2709=
XM_011525982.1:c.7962C>G	XP_011524284.1:p.Thr2654=
XM_011525978.2:c.8259C>G	XP_011524280.1:p.Thr2753=
XM_011525979.2:c.8250C>G	XP_011524281.1:p.Thr2750=
XM_011525980.2:c.8241C>G	XP_011524282.1:p.Thr2747=
XM_011525981.2:c.8127C>G	XP_011524283.1:p.Thr2709=
XM_011525982.2:c.7962C>G	XP_011524284.1:p.Thr2654=
XM_017025743.1:c.6111C>G	XP_016881232.1:p.Thr2037=
XM_017025744.1:c.3801C>G	XP_016881233.1:p.Thr1267=
XR_001753199.1:n.8500C>G
NM_000227.5:c.3405C>G	NP_000218.3:p.Thr1135=
NM_001127717.3:c.8064C>G	NP_001121189.2:p.Thr2688=
NM_001127718.3:c.3237C>G	NP_001121190.2:p.Thr1079=
NM_198129.3:c.8232C>G	NP_937762.2:p.Thr2744=
NM_000227.6:c.3405C>G MANE Plus Clinical	NP_000218.3:p.Thr1135=
NM_001127717.4:c.8064C>G	NP_001121189.2:p.Thr2688=
NM_001127718.4:c.3237C>G	NP_001121190.2:p.Thr1079=
NM_198129.4:c.8232C>G MANE Select	NP_937762.2:p.Thr2744=