Canonical Allele Identifier: CA402052034

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21530070C>A (hg19) ; chr18:g.23950106C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950106C>A , CM000680.2:g.23950106C>A	GRCh38
NC_000018.9:g.21530070C>A , CM000680.1:g.21530070C>A	GRCh37
NC_000018.8:g.19784068C>A	NCBI36
NG_007853.2:g.265509C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4762C>A MANE Plus Clinical	ENSP00000269217.5:p.His1588Asn
ENST00000313654.14:c.9589C>A MANE Select	ENSP00000324532.8:p.His3197Asn
ENST00000649721.1:c.6184C>A	ENSP00000497885.1:p.His2062Asn
ENST00000269217.10:c.4762C>A	ENSP00000269217.5:p.His1588Asn
ENST00000313654.13:c.9589C>A	ENSP00000324532.8:p.His3197Asn
ENST00000399516.7:c.9421C>A	ENSP00000382432.2:p.His3141Asn
ENST00000587184.5:c.4594C>A	ENSP00000466557.1:p.His1532Asn
ENST00000588004.1:c.110C>A
ENST00000588770.5:n.4167C>A
NM_000227.4:c.4762C>A	NP_000218.3:p.His1588Asn
NM_001127717.2:c.9421C>A	NP_001121189.2:p.His3141Asn
NM_001127718.2:c.4594C>A	NP_001121190.2:p.His1532Asn
NM_198129.2:c.9589C>A	NP_937762.2:p.His3197Asn
XM_011525978.1:c.9616C>A	XP_011524280.1:p.His3206Asn
XM_011525979.1:c.9607C>A	XP_011524281.1:p.His3203Asn
XM_011525980.1:c.9598C>A	XP_011524282.1:p.His3200Asn
XM_011525981.1:c.9484C>A	XP_011524283.1:p.His3162Asn
XM_011525982.1:c.9319C>A	XP_011524284.1:p.His3107Asn
XM_011525978.2:c.9616C>A	XP_011524280.1:p.His3206Asn
XM_011525979.2:c.9607C>A	XP_011524281.1:p.His3203Asn
XM_011525980.2:c.9598C>A	XP_011524282.1:p.His3200Asn
XM_011525981.2:c.9484C>A	XP_011524283.1:p.His3162Asn
XM_011525982.2:c.9319C>A	XP_011524284.1:p.His3107Asn
XM_017025743.1:c.7468C>A	XP_016881232.1:p.His2490Asn
XM_017025744.1:c.5158C>A	XP_016881233.1:p.His1720Asn
XR_001753199.1:n.9857C>A
NM_000227.5:c.4762C>A	NP_000218.3:p.His1588Asn
NM_001127717.3:c.9421C>A	NP_001121189.2:p.His3141Asn
NM_001127718.3:c.4594C>A	NP_001121190.2:p.His1532Asn
NM_198129.3:c.9589C>A	NP_937762.2:p.His3197Asn
NM_000227.6:c.4762C>A MANE Plus Clinical	NP_000218.3:p.His1588Asn
NM_001127717.4:c.9421C>A	NP_001121189.2:p.His3141Asn
NM_001127718.4:c.4594C>A	NP_001121190.2:p.His1532Asn
NM_198129.4:c.9589C>A MANE Select	NP_937762.2:p.His3197Asn