Canonical Allele Identifier: CA2290307517
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23864787T= , CM000680.2:g.23864787T= GRCh38
NC_000018.9:g.21444751T= , CM000680.1:g.21444751T= GRCh37
NC_000018.8:g.19698749T= NCBI36
NG_007853.2:g.180190T=

Transcript Alleles

HGVS Amino-acid change
ENST00000313654.14:c.4587T= MANE Select ENSP00000324532.8:p.Val1529=
ENST00000649721.1:c.1479T= ENSP00000497885.1:p.Val493=
ENST00000313654.13:c.4587T= ENSP00000324532.8:p.Val1529=
ENST00000399516.7:c.4587T= ENSP00000382432.2:p.Val1529=
NM_001127717.2:c.4587T= NP_001121189.2:p.Val1529=
NM_198129.2:c.4587T= NP_937762.2:p.Val1529=
XM_011525978.1:c.4614T= XP_011524280.1:p.Val1538=
XM_011525979.1:c.4605T= XP_011524281.1:p.Val1535=
XM_011525980.1:c.4596T= XP_011524282.1:p.Val1532=
XM_011525981.1:c.4482T= XP_011524283.1:p.Val1494=
XM_011525982.1:c.4614T= XP_011524284.1:p.Val1538=
XM_011525978.2:c.4614T= XP_011524280.1:p.Val1538=
XM_011525979.2:c.4605T= XP_011524281.1:p.Val1535=
XM_011525980.2:c.4596T= XP_011524282.1:p.Val1532=
XM_011525981.2:c.4482T= XP_011524283.1:p.Val1494=
XM_011525982.2:c.4614T= XP_011524284.1:p.Val1538=
XM_017025743.1:c.2466T= XP_016881232.1:p.Val822=
XM_017025744.1:c.156T= XP_016881233.1:p.Val52=
XR_001753199.1:n.4855T=
NM_001127717.3:c.4587T= NP_001121189.2:p.Val1529=
NM_198129.3:c.4587T= NP_937762.2:p.Val1529=
NM_001127717.4:c.4587T= NP_001121189.2:p.Val1529=
NM_198129.4:c.4587T= MANE Select NP_937762.2:p.Val1529=