Canonical Allele Identifier: CA402063116
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928174A>T , CM000680.2:g.23928174A>T GRCh38
NC_000018.9:g.21508138A>T , CM000680.1:g.21508138A>T GRCh37
NC_000018.8:g.19762136A>T NCBI36
NG_007853.2:g.243577A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.3402A>T MANE Plus Clinical ENSP00000269217.5:p.Lys1134Asn
ENST00000313654.14:c.8229A>T MANE Select ENSP00000324532.8:p.Lys2743Asn
ENST00000649721.1:c.4824A>T ENSP00000497885.1:p.Lys1608Asn
ENST00000269217.10:c.3402A>T ENSP00000269217.5:p.Lys1134Asn
ENST00000313654.13:c.8229A>T ENSP00000324532.8:p.Lys2743Asn
ENST00000399516.7:c.8061A>T ENSP00000382432.2:p.Lys2687Asn
ENST00000586751.5:c.3007A>T
ENST00000587184.5:c.3234A>T ENSP00000466557.1:p.Lys1078Asn
ENST00000588770.5:n.2807A>T
NM_000227.4:c.3402A>T NP_000218.3:p.Lys1134Asn
NM_001127717.2:c.8061A>T NP_001121189.2:p.Lys2687Asn
NM_001127718.2:c.3234A>T NP_001121190.2:p.Lys1078Asn
NM_198129.2:c.8229A>T NP_937762.2:p.Lys2743Asn
XM_011525978.1:c.8256A>T XP_011524280.1:p.Lys2752Asn
XM_011525979.1:c.8247A>T XP_011524281.1:p.Lys2749Asn
XM_011525980.1:c.8238A>T XP_011524282.1:p.Lys2746Asn
XM_011525981.1:c.8124A>T XP_011524283.1:p.Lys2708Asn
XM_011525982.1:c.7959A>T XP_011524284.1:p.Lys2653Asn
XM_011525978.2:c.8256A>T XP_011524280.1:p.Lys2752Asn
XM_011525979.2:c.8247A>T XP_011524281.1:p.Lys2749Asn
XM_011525980.2:c.8238A>T XP_011524282.1:p.Lys2746Asn
XM_011525981.2:c.8124A>T XP_011524283.1:p.Lys2708Asn
XM_011525982.2:c.7959A>T XP_011524284.1:p.Lys2653Asn
XM_017025743.1:c.6108A>T XP_016881232.1:p.Lys2036Asn
XM_017025744.1:c.3798A>T XP_016881233.1:p.Lys1266Asn
XR_001753199.1:n.8497A>T
NM_000227.5:c.3402A>T NP_000218.3:p.Lys1134Asn
NM_001127717.3:c.8061A>T NP_001121189.2:p.Lys2687Asn
NM_001127718.3:c.3234A>T NP_001121190.2:p.Lys1078Asn
NM_198129.3:c.8229A>T NP_937762.2:p.Lys2743Asn
NM_000227.6:c.3402A>T MANE Plus Clinical NP_000218.3:p.Lys1134Asn
NM_001127717.4:c.8061A>T NP_001121189.2:p.Lys2687Asn
NM_001127718.4:c.3234A>T NP_001121190.2:p.Lys1078Asn
NM_198129.4:c.8229A>T MANE Select NP_937762.2:p.Lys2743Asn