Canonical Allele Identifier: CA402051930

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21530021T>G (hg19) ; chr18:g.23950057T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950057T>G , CM000680.2:g.23950057T>G	GRCh38
NC_000018.9:g.21530021T>G , CM000680.1:g.21530021T>G	GRCh37
NC_000018.8:g.19784019T>G	NCBI36
NG_007853.2:g.265460T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4713T>G MANE Plus Clinical	ENSP00000269217.5:p.Phe1571Leu
ENST00000313654.14:c.9540T>G MANE Select	ENSP00000324532.8:p.Phe3180Leu
ENST00000649721.1:c.6135T>G	ENSP00000497885.1:p.Phe2045Leu
ENST00000269217.10:c.4713T>G	ENSP00000269217.5:p.Phe1571Leu
ENST00000313654.13:c.9540T>G	ENSP00000324532.8:p.Phe3180Leu
ENST00000399516.7:c.9372T>G	ENSP00000382432.2:p.Phe3124Leu
ENST00000587184.5:c.4545T>G	ENSP00000466557.1:p.Phe1515Leu
ENST00000588004.1:c.61T>G
ENST00000588770.5:n.4118T>G
NM_000227.4:c.4713T>G	NP_000218.3:p.Phe1571Leu
NM_001127717.2:c.9372T>G	NP_001121189.2:p.Phe3124Leu
NM_001127718.2:c.4545T>G	NP_001121190.2:p.Phe1515Leu
NM_198129.2:c.9540T>G	NP_937762.2:p.Phe3180Leu
XM_011525978.1:c.9567T>G	XP_011524280.1:p.Phe3189Leu
XM_011525979.1:c.9558T>G	XP_011524281.1:p.Phe3186Leu
XM_011525980.1:c.9549T>G	XP_011524282.1:p.Phe3183Leu
XM_011525981.1:c.9435T>G	XP_011524283.1:p.Phe3145Leu
XM_011525982.1:c.9270T>G	XP_011524284.1:p.Phe3090Leu
XM_011525978.2:c.9567T>G	XP_011524280.1:p.Phe3189Leu
XM_011525979.2:c.9558T>G	XP_011524281.1:p.Phe3186Leu
XM_011525980.2:c.9549T>G	XP_011524282.1:p.Phe3183Leu
XM_011525981.2:c.9435T>G	XP_011524283.1:p.Phe3145Leu
XM_011525982.2:c.9270T>G	XP_011524284.1:p.Phe3090Leu
XM_017025743.1:c.7419T>G	XP_016881232.1:p.Phe2473Leu
XM_017025744.1:c.5109T>G	XP_016881233.1:p.Phe1703Leu
XR_001753199.1:n.9808T>G
NM_000227.5:c.4713T>G	NP_000218.3:p.Phe1571Leu
NM_001127717.3:c.9372T>G	NP_001121189.2:p.Phe3124Leu
NM_001127718.3:c.4545T>G	NP_001121190.2:p.Phe1515Leu
NM_198129.3:c.9540T>G	NP_937762.2:p.Phe3180Leu
NM_000227.6:c.4713T>G MANE Plus Clinical	NP_000218.3:p.Phe1571Leu
NM_001127717.4:c.9372T>G	NP_001121189.2:p.Phe3124Leu
NM_001127718.4:c.4545T>G	NP_001121190.2:p.Phe1515Leu
NM_198129.4:c.9540T>G MANE Select	NP_937762.2:p.Phe3180Leu