Canonical Allele Identifier: CA402063934
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928676T>A , CM000680.2:g.23928676T>A GRCh38
NC_000018.9:g.21508640T>A , CM000680.1:g.21508640T>A GRCh37
NC_000018.8:g.19762638T>A NCBI36
NG_007853.2:g.244079T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.3520T>A MANE Plus Clinical ENSP00000269217.5:p.Leu1174Met
ENST00000313654.14:c.8347T>A MANE Select ENSP00000324532.8:p.Leu2783Met
ENST00000649721.1:c.4942T>A ENSP00000497885.1:p.Leu1648Met
ENST00000269217.10:c.3520T>A ENSP00000269217.5:p.Leu1174Met
ENST00000313654.13:c.8347T>A ENSP00000324532.8:p.Leu2783Met
ENST00000399516.7:c.8179T>A ENSP00000382432.2:p.Leu2727Met
ENST00000586751.5:c.3125T>A
ENST00000587184.5:c.3352T>A ENSP00000466557.1:p.Leu1118Met
ENST00000588164.2:c.52T>A ENSP00000467473.2:p.Leu18Met
ENST00000588770.5:n.2925T>A
NM_000227.4:c.3520T>A NP_000218.3:p.Leu1174Met
NM_001127717.2:c.8179T>A NP_001121189.2:p.Leu2727Met
NM_001127718.2:c.3352T>A NP_001121190.2:p.Leu1118Met
NM_198129.2:c.8347T>A NP_937762.2:p.Leu2783Met
XM_011525978.1:c.8374T>A XP_011524280.1:p.Leu2792Met
XM_011525979.1:c.8365T>A XP_011524281.1:p.Leu2789Met
XM_011525980.1:c.8356T>A XP_011524282.1:p.Leu2786Met
XM_011525981.1:c.8242T>A XP_011524283.1:p.Leu2748Met
XM_011525982.1:c.8077T>A XP_011524284.1:p.Leu2693Met
XM_011525978.2:c.8374T>A XP_011524280.1:p.Leu2792Met
XM_011525979.2:c.8365T>A XP_011524281.1:p.Leu2789Met
XM_011525980.2:c.8356T>A XP_011524282.1:p.Leu2786Met
XM_011525981.2:c.8242T>A XP_011524283.1:p.Leu2748Met
XM_011525982.2:c.8077T>A XP_011524284.1:p.Leu2693Met
XM_017025743.1:c.6226T>A XP_016881232.1:p.Leu2076Met
XM_017025744.1:c.3916T>A XP_016881233.1:p.Leu1306Met
XR_001753199.1:n.8615T>A
NM_000227.5:c.3520T>A NP_000218.3:p.Leu1174Met
NM_001127717.3:c.8179T>A NP_001121189.2:p.Leu2727Met
NM_001127718.3:c.3352T>A NP_001121190.2:p.Leu1118Met
NM_198129.3:c.8347T>A NP_937762.2:p.Leu2783Met
NM_000227.6:c.3520T>A MANE Plus Clinical NP_000218.3:p.Leu1174Met
NM_001127717.4:c.8179T>A NP_001121189.2:p.Leu2727Met
NM_001127718.4:c.3352T>A NP_001121190.2:p.Leu1118Met
NM_198129.4:c.8347T>A MANE Select NP_937762.2:p.Leu2783Met