Canonical Allele Identifier: CA503327964
Gene: LAMA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.21456371T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23876407T>C , CM000680.2:g.23876407T>C GRCh38
NC_000018.9:g.21456371T>C , CM000680.1:g.21456371T>C GRCh37
NC_000018.8:g.19710369T>C NCBI36
NG_007853.2:g.191810T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.285T>C MANE Plus Clinical ENSP00000269217.5:p.Val95=
ENST00000313654.14:c.5112T>C MANE Select ENSP00000324532.8:p.Val1704=
ENST00000649721.1:c.2004T>C ENSP00000497885.1:p.Val668=
ENST00000269217.10:c.285T>C ENSP00000269217.5:p.Val95=
ENST00000313654.13:c.5112T>C ENSP00000324532.8:p.Val1704=
ENST00000399516.7:c.5112T>C ENSP00000382432.2:p.Val1704=
ENST00000587184.5:c.285T>C ENSP00000466557.1:p.Val95=
NM_000227.4:c.285T>C NP_000218.3:p.Val95=
NM_001127717.2:c.5112T>C NP_001121189.2:p.Val1704=
NM_001127718.2:c.285T>C NP_001121190.2:p.Val95=
NM_198129.2:c.5112T>C NP_937762.2:p.Val1704=
XM_011525978.1:c.5139T>C XP_011524280.1:p.Val1713=
XM_011525979.1:c.5130T>C XP_011524281.1:p.Val1710=
XM_011525980.1:c.5121T>C XP_011524282.1:p.Val1707=
XM_011525981.1:c.5007T>C XP_011524283.1:p.Val1669=
XM_011525982.1:c.5139T>C XP_011524284.1:p.Val1713=
XM_011525978.2:c.5139T>C XP_011524280.1:p.Val1713=
XM_011525979.2:c.5130T>C XP_011524281.1:p.Val1710=
XM_011525980.2:c.5121T>C XP_011524282.1:p.Val1707=
XM_011525981.2:c.5007T>C XP_011524283.1:p.Val1669=
XM_011525982.2:c.5139T>C XP_011524284.1:p.Val1713=
XM_017025743.1:c.2991T>C XP_016881232.1:p.Val997=
XM_017025744.1:c.681T>C XP_016881233.1:p.Val227=
XR_001753199.1:n.5380T>C
NM_000227.5:c.285T>C NP_000218.3:p.Val95=
NM_001127717.3:c.5112T>C NP_001121189.2:p.Val1704=
NM_001127718.3:c.285T>C NP_001121190.2:p.Val95=
NM_198129.3:c.5112T>C NP_937762.2:p.Val1704=
NM_000227.6:c.285T>C MANE Plus Clinical NP_000218.3:p.Val95=
NM_001127717.4:c.5112T>C NP_001121189.2:p.Val1704=
NM_001127718.4:c.285T>C NP_001121190.2:p.Val95=
NM_198129.4:c.5112T>C MANE Select NP_937762.2:p.Val1704=