Canonical Allele Identifier: CA402059272

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495338T>G (hg19) ; chr18:g.23915374T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915374T>G , CM000680.2:g.23915374T>G	GRCh38
NC_000018.9:g.21495338T>G , CM000680.1:g.21495338T>G	GRCh37
NC_000018.8:g.19749336T>G	NCBI36
NG_007853.2:g.230777T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2903T>G MANE Plus Clinical	ENSP00000269217.5:p.Phe968Cys
ENST00000313654.14:c.7730T>G MANE Select	ENSP00000324532.8:p.Phe2577Cys
ENST00000649721.1:c.4325T>G	ENSP00000497885.1:p.Phe1442Cys
ENST00000269217.10:c.2903T>G	ENSP00000269217.5:p.Phe968Cys
ENST00000313654.13:c.7730T>G	ENSP00000324532.8:p.Phe2577Cys
ENST00000399516.7:c.7562T>G	ENSP00000382432.2:p.Phe2521Cys
ENST00000586751.5:c.2508T>G
ENST00000587184.5:c.2735T>G	ENSP00000466557.1:p.Phe912Cys
ENST00000588770.5:n.2308T>G
NM_000227.4:c.2903T>G	NP_000218.3:p.Phe968Cys
NM_001127717.2:c.7562T>G	NP_001121189.2:p.Phe2521Cys
NM_001127718.2:c.2735T>G	NP_001121190.2:p.Phe912Cys
NM_198129.2:c.7730T>G	NP_937762.2:p.Phe2577Cys
XM_011525978.1:c.7757T>G	XP_011524280.1:p.Phe2586Cys
XM_011525979.1:c.7748T>G	XP_011524281.1:p.Phe2583Cys
XM_011525980.1:c.7739T>G	XP_011524282.1:p.Phe2580Cys
XM_011525981.1:c.7625T>G	XP_011524283.1:p.Phe2542Cys
XM_011525982.1:c.7460T>G	XP_011524284.1:p.Phe2487Cys
XM_011525978.2:c.7757T>G	XP_011524280.1:p.Phe2586Cys
XM_011525979.2:c.7748T>G	XP_011524281.1:p.Phe2583Cys
XM_011525980.2:c.7739T>G	XP_011524282.1:p.Phe2580Cys
XM_011525981.2:c.7625T>G	XP_011524283.1:p.Phe2542Cys
XM_011525982.2:c.7460T>G	XP_011524284.1:p.Phe2487Cys
XM_017025743.1:c.5609T>G	XP_016881232.1:p.Phe1870Cys
XM_017025744.1:c.3299T>G	XP_016881233.1:p.Phe1100Cys
XR_001753199.1:n.7998T>G
NM_000227.5:c.2903T>G	NP_000218.3:p.Phe968Cys
NM_001127717.3:c.7562T>G	NP_001121189.2:p.Phe2521Cys
NM_001127718.3:c.2735T>G	NP_001121190.2:p.Phe912Cys
NM_198129.3:c.7730T>G	NP_937762.2:p.Phe2577Cys
NM_000227.6:c.2903T>G MANE Plus Clinical	NP_000218.3:p.Phe968Cys
NM_001127717.4:c.7562T>G	NP_001121189.2:p.Phe2521Cys
NM_001127718.4:c.2735T>G	NP_001121190.2:p.Phe912Cys
NM_198129.4:c.7730T>G MANE Select	NP_937762.2:p.Phe2577Cys