Canonical Allele Identifier: CA2290334854
Community Standard Title: NM_198129.4(LAMA3):c.8436G= (p.Trp2812=)
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928765G= , CM000680.2:g.23928765G= GRCh38
NC_000018.9:g.21508729G= , CM000680.1:g.21508729G= GRCh37
NC_000018.8:g.19762727G= NCBI36
NG_007853.2:g.244168G=

Transcript Alleles

HGVS Amino-acid Change
NM_198129.4:c.8436G= MANE Select NP_937762.2:p.Trp2812=
ENST00000313654.14:c.8436G= MANE Select ENSP00000324532.8:p.Trp2812=
NM_000227.6:c.3609G= MANE Plus Clinical NP_000218.3:p.Trp1203=
ENST00000269217.11:c.3609G= MANE Plus Clinical ENSP00000269217.5:p.Trp1203=
NM_000227.4:c.3609G= NP_000218.3:p.Trp1203=
NM_000227.5:c.3609G= NP_000218.3:p.Trp1203=
NM_001127717.2:c.8268G= NP_001121189.2:p.Trp2756=
NM_001127717.3:c.8268G= NP_001121189.2:p.Trp2756=
NM_001127717.4:c.8268G= NP_001121189.2:p.Trp2756=
NM_001127718.2:c.3441G= NP_001121190.2:p.Trp1147=
NM_001127718.3:c.3441G= NP_001121190.2:p.Trp1147=
NM_001127718.4:c.3441G= NP_001121190.2:p.Trp1147=
NM_198129.2:c.8436G= NP_937762.2:p.Trp2812=
NM_198129.3:c.8436G= NP_937762.2:p.Trp2812=
ENST00000269217.10:c.3609G= ENSP00000269217.5:p.Trp1203=
ENST00000313654.13:c.8436G= ENSP00000324532.8:p.Trp2812=
ENST00000399516.7:c.8268G= ENSP00000382432.2:p.Trp2756=
ENST00000586751.5:c.3214G=
ENST00000587184.5:c.3441G= ENSP00000466557.1:p.Trp1147=
ENST00000588164.2:c.141G= ENSP00000467473.2:p.Trp47=
ENST00000588770.5:n.3014G=
ENST00000649721.1:c.5031G= ENSP00000497885.1:p.Trp1677=
XM_011525978.1:c.8463G= XP_011524280.1:p.Trp2821=
XM_011525978.2:c.8463G= XP_011524280.1:p.Trp2821=
XM_011525979.1:c.8454G= XP_011524281.1:p.Trp2818=
XM_011525979.2:c.8454G= XP_011524281.1:p.Trp2818=
XM_011525980.1:c.8445G= XP_011524282.1:p.Trp2815=
XM_011525980.2:c.8445G= XP_011524282.1:p.Trp2815=
XM_011525981.1:c.8331G= XP_011524283.1:p.Trp2777=
XM_011525981.2:c.8331G= XP_011524283.1:p.Trp2777=
XM_011525982.1:c.8166G= XP_011524284.1:p.Trp2722=
XM_011525982.2:c.8166G= XP_011524284.1:p.Trp2722=
XM_017025743.1:c.6315G= XP_016881232.1:p.Trp2105=
XM_017025744.1:c.4005G= XP_016881233.1:p.Trp1335=
XR_001753199.1:n.8704G=