Canonical Allele Identifier: CA402051881

Gene: LAMA3

Linked Data

• dbSNP Id: rs2082850515
• MyVariant Identifiers: chr18:g.21529998T>C (hg19) ; chr18:g.23950034T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950034T>C , CM000680.2:g.23950034T>C	GRCh38
NC_000018.9:g.21529998T>C , CM000680.1:g.21529998T>C	GRCh37
NC_000018.8:g.19783996T>C	NCBI36
NG_007853.2:g.265437T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4690T>C MANE Plus Clinical	ENSP00000269217.5:p.Ser1564Pro
ENST00000313654.14:c.9517T>C MANE Select	ENSP00000324532.8:p.Ser3173Pro
ENST00000649721.1:c.6112T>C	ENSP00000497885.1:p.Ser2038Pro
ENST00000269217.10:c.4690T>C	ENSP00000269217.5:p.Ser1564Pro
ENST00000313654.13:c.9517T>C	ENSP00000324532.8:p.Ser3173Pro
ENST00000399516.7:c.9349T>C	ENSP00000382432.2:p.Ser3117Pro
ENST00000587184.5:c.4522T>C	ENSP00000466557.1:p.Ser1508Pro
ENST00000588004.1:c.38T>C
ENST00000588770.5:n.4095T>C
NM_000227.4:c.4690T>C	NP_000218.3:p.Ser1564Pro
NM_001127717.2:c.9349T>C	NP_001121189.2:p.Ser3117Pro
NM_001127718.2:c.4522T>C	NP_001121190.2:p.Ser1508Pro
NM_198129.2:c.9517T>C	NP_937762.2:p.Ser3173Pro
XM_011525978.1:c.9544T>C	XP_011524280.1:p.Ser3182Pro
XM_011525979.1:c.9535T>C	XP_011524281.1:p.Ser3179Pro
XM_011525980.1:c.9526T>C	XP_011524282.1:p.Ser3176Pro
XM_011525981.1:c.9412T>C	XP_011524283.1:p.Ser3138Pro
XM_011525982.1:c.9247T>C	XP_011524284.1:p.Ser3083Pro
XM_011525978.2:c.9544T>C	XP_011524280.1:p.Ser3182Pro
XM_011525979.2:c.9535T>C	XP_011524281.1:p.Ser3179Pro
XM_011525980.2:c.9526T>C	XP_011524282.1:p.Ser3176Pro
XM_011525981.2:c.9412T>C	XP_011524283.1:p.Ser3138Pro
XM_011525982.2:c.9247T>C	XP_011524284.1:p.Ser3083Pro
XM_017025743.1:c.7396T>C	XP_016881232.1:p.Ser2466Pro
XM_017025744.1:c.5086T>C	XP_016881233.1:p.Ser1696Pro
XR_001753199.1:n.9785T>C
NM_000227.5:c.4690T>C	NP_000218.3:p.Ser1564Pro
NM_001127717.3:c.9349T>C	NP_001121189.2:p.Ser3117Pro
NM_001127718.3:c.4522T>C	NP_001121190.2:p.Ser1508Pro
NM_198129.3:c.9517T>C	NP_937762.2:p.Ser3173Pro
NM_000227.6:c.4690T>C MANE Plus Clinical	NP_000218.3:p.Ser1564Pro
NM_001127717.4:c.9349T>C	NP_001121189.2:p.Ser3117Pro
NM_001127718.4:c.4522T>C	NP_001121190.2:p.Ser1508Pro
NM_198129.4:c.9517T>C MANE Select	NP_937762.2:p.Ser3173Pro