Canonical Allele Identifier: CA402063062

Gene: LAMA3

Linked Data

• dbSNP Id: rs1235636159
• MyVariant Identifiers: chr18:g.21508128A>C (hg19) ; chr18:g.23928164A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928164A>C , CM000680.2:g.23928164A>C	GRCh38
NC_000018.9:g.21508128A>C , CM000680.1:g.21508128A>C	GRCh37
NC_000018.8:g.19762126A>C	NCBI36
NG_007853.2:g.243567A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3392A>C MANE Plus Clinical	ENSP00000269217.5:p.Asn1131Thr
ENST00000313654.14:c.8219A>C MANE Select	ENSP00000324532.8:p.Asn2740Thr
ENST00000649721.1:c.4814A>C	ENSP00000497885.1:p.Asn1605Thr
ENST00000269217.10:c.3392A>C	ENSP00000269217.5:p.Asn1131Thr
ENST00000313654.13:c.8219A>C	ENSP00000324532.8:p.Asn2740Thr
ENST00000399516.7:c.8051A>C	ENSP00000382432.2:p.Asn2684Thr
ENST00000586751.5:c.2997A>C
ENST00000587184.5:c.3224A>C	ENSP00000466557.1:p.Asn1075Thr
ENST00000588770.5:n.2797A>C
NM_000227.4:c.3392A>C	NP_000218.3:p.Asn1131Thr
NM_001127717.2:c.8051A>C	NP_001121189.2:p.Asn2684Thr
NM_001127718.2:c.3224A>C	NP_001121190.2:p.Asn1075Thr
NM_198129.2:c.8219A>C	NP_937762.2:p.Asn2740Thr
XM_011525978.1:c.8246A>C	XP_011524280.1:p.Asn2749Thr
XM_011525979.1:c.8237A>C	XP_011524281.1:p.Asn2746Thr
XM_011525980.1:c.8228A>C	XP_011524282.1:p.Asn2743Thr
XM_011525981.1:c.8114A>C	XP_011524283.1:p.Asn2705Thr
XM_011525982.1:c.7949A>C	XP_011524284.1:p.Asn2650Thr
XM_011525978.2:c.8246A>C	XP_011524280.1:p.Asn2749Thr
XM_011525979.2:c.8237A>C	XP_011524281.1:p.Asn2746Thr
XM_011525980.2:c.8228A>C	XP_011524282.1:p.Asn2743Thr
XM_011525981.2:c.8114A>C	XP_011524283.1:p.Asn2705Thr
XM_011525982.2:c.7949A>C	XP_011524284.1:p.Asn2650Thr
XM_017025743.1:c.6098A>C	XP_016881232.1:p.Asn2033Thr
XM_017025744.1:c.3788A>C	XP_016881233.1:p.Asn1263Thr
XR_001753199.1:n.8487A>C
NM_000227.5:c.3392A>C	NP_000218.3:p.Asn1131Thr
NM_001127717.3:c.8051A>C	NP_001121189.2:p.Asn2684Thr
NM_001127718.3:c.3224A>C	NP_001121190.2:p.Asn1075Thr
NM_198129.3:c.8219A>C	NP_937762.2:p.Asn2740Thr
NM_000227.6:c.3392A>C MANE Plus Clinical	NP_000218.3:p.Asn1131Thr
NM_001127717.4:c.8051A>C	NP_001121189.2:p.Asn2684Thr
NM_001127718.4:c.3224A>C	NP_001121190.2:p.Asn1075Thr
NM_198129.4:c.8219A>C MANE Select	NP_937762.2:p.Asn2740Thr