Canonical Allele Identifier: CA402063311

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508179C>G (hg19) ; chr18:g.23928215C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928215C>G , CM000680.2:g.23928215C>G	GRCh38
NC_000018.9:g.21508179C>G , CM000680.1:g.21508179C>G	GRCh37
NC_000018.8:g.19762177C>G	NCBI36
NG_007853.2:g.243618C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3443C>G MANE Plus Clinical	ENSP00000269217.5:p.Thr1148Ser
ENST00000313654.14:c.8270C>G MANE Select	ENSP00000324532.8:p.Thr2757Ser
ENST00000649721.1:c.4865C>G	ENSP00000497885.1:p.Thr1622Ser
ENST00000269217.10:c.3443C>G	ENSP00000269217.5:p.Thr1148Ser
ENST00000313654.13:c.8270C>G	ENSP00000324532.8:p.Thr2757Ser
ENST00000399516.7:c.8102C>G	ENSP00000382432.2:p.Thr2701Ser
ENST00000586751.5:c.3048C>G
ENST00000587184.5:c.3275C>G	ENSP00000466557.1:p.Thr1092Ser
ENST00000588770.5:n.2848C>G
NM_000227.4:c.3443C>G	NP_000218.3:p.Thr1148Ser
NM_001127717.2:c.8102C>G	NP_001121189.2:p.Thr2701Ser
NM_001127718.2:c.3275C>G	NP_001121190.2:p.Thr1092Ser
NM_198129.2:c.8270C>G	NP_937762.2:p.Thr2757Ser
XM_011525978.1:c.8297C>G	XP_011524280.1:p.Thr2766Ser
XM_011525979.1:c.8288C>G	XP_011524281.1:p.Thr2763Ser
XM_011525980.1:c.8279C>G	XP_011524282.1:p.Thr2760Ser
XM_011525981.1:c.8165C>G	XP_011524283.1:p.Thr2722Ser
XM_011525982.1:c.8000C>G	XP_011524284.1:p.Thr2667Ser
XM_011525978.2:c.8297C>G	XP_011524280.1:p.Thr2766Ser
XM_011525979.2:c.8288C>G	XP_011524281.1:p.Thr2763Ser
XM_011525980.2:c.8279C>G	XP_011524282.1:p.Thr2760Ser
XM_011525981.2:c.8165C>G	XP_011524283.1:p.Thr2722Ser
XM_011525982.2:c.8000C>G	XP_011524284.1:p.Thr2667Ser
XM_017025743.1:c.6149C>G	XP_016881232.1:p.Thr2050Ser
XM_017025744.1:c.3839C>G	XP_016881233.1:p.Thr1280Ser
XR_001753199.1:n.8538C>G
NM_000227.5:c.3443C>G	NP_000218.3:p.Thr1148Ser
NM_001127717.3:c.8102C>G	NP_001121189.2:p.Thr2701Ser
NM_001127718.3:c.3275C>G	NP_001121190.2:p.Thr1092Ser
NM_198129.3:c.8270C>G	NP_937762.2:p.Thr2757Ser
NM_000227.6:c.3443C>G MANE Plus Clinical	NP_000218.3:p.Thr1148Ser
NM_001127717.4:c.8102C>G	NP_001121189.2:p.Thr2701Ser
NM_001127718.4:c.3275C>G	NP_001121190.2:p.Thr1092Ser
NM_198129.4:c.8270C>G MANE Select	NP_937762.2:p.Thr2757Ser