Canonical Allele Identifier: CA503340783

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508645C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928681C>A , CM000680.2:g.23928681C>A	GRCh38
NC_000018.9:g.21508645C>A , CM000680.1:g.21508645C>A	GRCh37
NC_000018.8:g.19762643C>A	NCBI36
NG_007853.2:g.244084C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3525C>A MANE Plus Clinical	ENSP00000269217.5:p.Gly1175=
ENST00000313654.14:c.8352C>A MANE Select	ENSP00000324532.8:p.Gly2784=
ENST00000649721.1:c.4947C>A	ENSP00000497885.1:p.Gly1649=
ENST00000269217.10:c.3525C>A	ENSP00000269217.5:p.Gly1175=
ENST00000313654.13:c.8352C>A	ENSP00000324532.8:p.Gly2784=
ENST00000399516.7:c.8184C>A	ENSP00000382432.2:p.Gly2728=
ENST00000586751.5:c.3130C>A
ENST00000587184.5:c.3357C>A	ENSP00000466557.1:p.Gly1119=
ENST00000588164.2:c.57C>A	ENSP00000467473.2:p.Gly19=
ENST00000588770.5:n.2930C>A
NM_000227.4:c.3525C>A	NP_000218.3:p.Gly1175=
NM_001127717.2:c.8184C>A	NP_001121189.2:p.Gly2728=
NM_001127718.2:c.3357C>A	NP_001121190.2:p.Gly1119=
NM_198129.2:c.8352C>A	NP_937762.2:p.Gly2784=
XM_011525978.1:c.8379C>A	XP_011524280.1:p.Gly2793=
XM_011525979.1:c.8370C>A	XP_011524281.1:p.Gly2790=
XM_011525980.1:c.8361C>A	XP_011524282.1:p.Gly2787=
XM_011525981.1:c.8247C>A	XP_011524283.1:p.Gly2749=
XM_011525982.1:c.8082C>A	XP_011524284.1:p.Gly2694=
XM_011525978.2:c.8379C>A	XP_011524280.1:p.Gly2793=
XM_011525979.2:c.8370C>A	XP_011524281.1:p.Gly2790=
XM_011525980.2:c.8361C>A	XP_011524282.1:p.Gly2787=
XM_011525981.2:c.8247C>A	XP_011524283.1:p.Gly2749=
XM_011525982.2:c.8082C>A	XP_011524284.1:p.Gly2694=
XM_017025743.1:c.6231C>A	XP_016881232.1:p.Gly2077=
XM_017025744.1:c.3921C>A	XP_016881233.1:p.Gly1307=
XR_001753199.1:n.8620C>A
NM_000227.5:c.3525C>A	NP_000218.3:p.Gly1175=
NM_001127717.3:c.8184C>A	NP_001121189.2:p.Gly2728=
NM_001127718.3:c.3357C>A	NP_001121190.2:p.Gly1119=
NM_198129.3:c.8352C>A	NP_937762.2:p.Gly2784=
NM_000227.6:c.3525C>A MANE Plus Clinical	NP_000218.3:p.Gly1175=
NM_001127717.4:c.8184C>A	NP_001121189.2:p.Gly2728=
NM_001127718.4:c.3357C>A	NP_001121190.2:p.Gly1119=
NM_198129.4:c.8352C>A MANE Select	NP_937762.2:p.Gly2784=