Canonical Allele Identifier: CA402063902

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508632T>A (hg19) ; chr18:g.23928668T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928668T>A , CM000680.2:g.23928668T>A	GRCh38
NC_000018.9:g.21508632T>A , CM000680.1:g.21508632T>A	GRCh37
NC_000018.8:g.19762630T>A	NCBI36
NG_007853.2:g.244071T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3512T>A MANE Plus Clinical	ENSP00000269217.5:p.Phe1171Tyr
ENST00000313654.14:c.8339T>A MANE Select	ENSP00000324532.8:p.Phe2780Tyr
ENST00000649721.1:c.4934T>A	ENSP00000497885.1:p.Phe1645Tyr
ENST00000269217.10:c.3512T>A	ENSP00000269217.5:p.Phe1171Tyr
ENST00000313654.13:c.8339T>A	ENSP00000324532.8:p.Phe2780Tyr
ENST00000399516.7:c.8171T>A	ENSP00000382432.2:p.Phe2724Tyr
ENST00000586751.5:c.3117T>A
ENST00000587184.5:c.3344T>A	ENSP00000466557.1:p.Phe1115Tyr
ENST00000588164.2:c.44T>A	ENSP00000467473.2:p.Phe15Tyr
ENST00000588770.5:n.2917T>A
NM_000227.4:c.3512T>A	NP_000218.3:p.Phe1171Tyr
NM_001127717.2:c.8171T>A	NP_001121189.2:p.Phe2724Tyr
NM_001127718.2:c.3344T>A	NP_001121190.2:p.Phe1115Tyr
NM_198129.2:c.8339T>A	NP_937762.2:p.Phe2780Tyr
XM_011525978.1:c.8366T>A	XP_011524280.1:p.Phe2789Tyr
XM_011525979.1:c.8357T>A	XP_011524281.1:p.Phe2786Tyr
XM_011525980.1:c.8348T>A	XP_011524282.1:p.Phe2783Tyr
XM_011525981.1:c.8234T>A	XP_011524283.1:p.Phe2745Tyr
XM_011525982.1:c.8069T>A	XP_011524284.1:p.Phe2690Tyr
XM_011525978.2:c.8366T>A	XP_011524280.1:p.Phe2789Tyr
XM_011525979.2:c.8357T>A	XP_011524281.1:p.Phe2786Tyr
XM_011525980.2:c.8348T>A	XP_011524282.1:p.Phe2783Tyr
XM_011525981.2:c.8234T>A	XP_011524283.1:p.Phe2745Tyr
XM_011525982.2:c.8069T>A	XP_011524284.1:p.Phe2690Tyr
XM_017025743.1:c.6218T>A	XP_016881232.1:p.Phe2073Tyr
XM_017025744.1:c.3908T>A	XP_016881233.1:p.Phe1303Tyr
XR_001753199.1:n.8607T>A
NM_000227.5:c.3512T>A	NP_000218.3:p.Phe1171Tyr
NM_001127717.3:c.8171T>A	NP_001121189.2:p.Phe2724Tyr
NM_001127718.3:c.3344T>A	NP_001121190.2:p.Phe1115Tyr
NM_198129.3:c.8339T>A	NP_937762.2:p.Phe2780Tyr
NM_000227.6:c.3512T>A MANE Plus Clinical	NP_000218.3:p.Phe1171Tyr
NM_001127717.4:c.8171T>A	NP_001121189.2:p.Phe2724Tyr
NM_001127718.4:c.3344T>A	NP_001121190.2:p.Phe1115Tyr
NM_198129.4:c.8339T>A MANE Select	NP_937762.2:p.Phe2780Tyr