Canonical Allele Identifier: CA8917248
Gene: LAMA3 HGNC NCBI

Linked Data

dbSNP Id: rs779131897

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23950159G>T , CM000680.2:g.23950159G>T GRCh38
NC_000018.9:g.21530123G>T , CM000680.1:g.21530123G>T GRCh37
NC_000018.8:g.19784121G>T NCBI36
NG_007853.2:g.265562G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.4815G>T MANE Plus Clinical ENSP00000269217.5:p.Lys1605Asn
ENST00000313654.14:c.9642G>T MANE Select ENSP00000324532.8:p.Lys3214Asn
ENST00000649721.1:n.6237G>T ENSP00000497885.1:p.Lys2079Asn
ENST00000269217.10:c.4815G>T ENSP00000269217.5:p.Lys1605Asn
ENST00000313654.13:c.9642G>T ENSP00000324532.8:p.Lys3214Asn
ENST00000399516.7:n.9474G>T ENSP00000382432.2:p.Lys3158Asn
ENST00000587184.5:n.4647G>T ENSP00000466557.1:p.Lys1549Asn
ENST00000588004.1:n.163G>T
ENST00000588770.5:n.4220G>T
NM_000227.4:c.4815G>T NP_000218.3:p.Lys1605Asn
NM_001127717.2:c.9474G>T NP_001121189.2:p.Lys3158Asn
NM_001127718.2:c.4647G>T NP_001121190.2:p.Lys1549Asn
NM_198129.2:c.9642G>T NP_937762.2:p.Lys3214Asn
XM_011525978.1:c.9669G>T XP_011524280.1:p.Lys3223Asn
XM_011525979.1:c.9660G>T XP_011524281.1:p.Lys3220Asn
XM_011525980.1:c.9651G>T XP_011524282.1:p.Lys3217Asn
XM_011525981.1:c.9537G>T XP_011524283.1:p.Lys3179Asn
XM_011525982.1:c.9372G>T XP_011524284.1:p.Lys3124Asn
XM_011525978.2:c.9669G>T XP_011524280.1:p.Lys3223Asn
XM_011525979.2:c.9660G>T XP_011524281.1:p.Lys3220Asn
XM_011525980.2:c.9651G>T XP_011524282.1:p.Lys3217Asn
XM_011525981.2:c.9537G>T XP_011524283.1:p.Lys3179Asn
XM_011525982.2:c.9372G>T XP_011524284.1:p.Lys3124Asn
XM_017025743.1:c.7521G>T XP_016881232.1:p.Lys2507Asn
XM_017025744.1:c.5211G>T XP_016881233.1:p.Lys1737Asn
XR_001753199.1:n.9910G>T
NM_000227.5:c.4815G>T NP_000218.3:p.Lys1605Asn
NM_001127717.3:c.9474G>T NP_001121189.2:p.Lys3158Asn
NM_001127718.3:c.4647G>T NP_001121190.2:p.Lys1549Asn
NM_198129.3:c.9642G>T NP_937762.2:p.Lys3214Asn
NM_000227.6:c.4815G>T MANE Plus Clinical NP_000218.3:p.Lys1605Asn
NM_001127717.4:c.9474G>T NP_001121189.2:p.Lys3158Asn
NM_001127718.4:c.4647G>T NP_001121190.2:p.Lys1549Asn
NM_198129.4:c.9642G>T MANE Select NP_937762.2:p.Lys3214Asn