Canonical Allele Identifier: CA402063288

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508173G>C (hg19) ; chr18:g.23928209G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928209G>C , CM000680.2:g.23928209G>C	GRCh38
NC_000018.9:g.21508173G>C , CM000680.1:g.21508173G>C	GRCh37
NC_000018.8:g.19762171G>C	NCBI36
NG_007853.2:g.243612G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3437G>C MANE Plus Clinical	ENSP00000269217.5:p.Gly1146Ala
ENST00000313654.14:c.8264G>C MANE Select	ENSP00000324532.8:p.Gly2755Ala
ENST00000649721.1:c.4859G>C	ENSP00000497885.1:p.Gly1620Ala
ENST00000269217.10:c.3437G>C	ENSP00000269217.5:p.Gly1146Ala
ENST00000313654.13:c.8264G>C	ENSP00000324532.8:p.Gly2755Ala
ENST00000399516.7:c.8096G>C	ENSP00000382432.2:p.Gly2699Ala
ENST00000586751.5:c.3042G>C
ENST00000587184.5:c.3269G>C	ENSP00000466557.1:p.Gly1090Ala
ENST00000588770.5:n.2842G>C
NM_000227.4:c.3437G>C	NP_000218.3:p.Gly1146Ala
NM_001127717.2:c.8096G>C	NP_001121189.2:p.Gly2699Ala
NM_001127718.2:c.3269G>C	NP_001121190.2:p.Gly1090Ala
NM_198129.2:c.8264G>C	NP_937762.2:p.Gly2755Ala
XM_011525978.1:c.8291G>C	XP_011524280.1:p.Gly2764Ala
XM_011525979.1:c.8282G>C	XP_011524281.1:p.Gly2761Ala
XM_011525980.1:c.8273G>C	XP_011524282.1:p.Gly2758Ala
XM_011525981.1:c.8159G>C	XP_011524283.1:p.Gly2720Ala
XM_011525982.1:c.7994G>C	XP_011524284.1:p.Gly2665Ala
XM_011525978.2:c.8291G>C	XP_011524280.1:p.Gly2764Ala
XM_011525979.2:c.8282G>C	XP_011524281.1:p.Gly2761Ala
XM_011525980.2:c.8273G>C	XP_011524282.1:p.Gly2758Ala
XM_011525981.2:c.8159G>C	XP_011524283.1:p.Gly2720Ala
XM_011525982.2:c.7994G>C	XP_011524284.1:p.Gly2665Ala
XM_017025743.1:c.6143G>C	XP_016881232.1:p.Gly2048Ala
XM_017025744.1:c.3833G>C	XP_016881233.1:p.Gly1278Ala
XR_001753199.1:n.8532G>C
NM_000227.5:c.3437G>C	NP_000218.3:p.Gly1146Ala
NM_001127717.3:c.8096G>C	NP_001121189.2:p.Gly2699Ala
NM_001127718.3:c.3269G>C	NP_001121190.2:p.Gly1090Ala
NM_198129.3:c.8264G>C	NP_937762.2:p.Gly2755Ala
NM_000227.6:c.3437G>C MANE Plus Clinical	NP_000218.3:p.Gly1146Ala
NM_001127717.4:c.8096G>C	NP_001121189.2:p.Gly2699Ala
NM_001127718.4:c.3269G>C	NP_001121190.2:p.Gly1090Ala
NM_198129.4:c.8264G>C MANE Select	NP_937762.2:p.Gly2755Ala