Canonical Allele Identifier: CA2290312361
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23876394C= , CM000680.2:g.23876394C= GRCh38
NC_000018.9:g.21456358C= , CM000680.1:g.21456358C= GRCh37
NC_000018.8:g.19710356C= NCBI36
NG_007853.2:g.191797C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.272C= MANE Plus Clinical ENSP00000269217.5:p.Ser91=
ENST00000313654.14:c.5099C= MANE Select ENSP00000324532.8:p.Ser1700=
ENST00000649721.1:c.1991C= ENSP00000497885.1:p.Ser664=
ENST00000269217.10:c.272C= ENSP00000269217.5:p.Ser91=
ENST00000313654.13:c.5099C= ENSP00000324532.8:p.Ser1700=
ENST00000399516.7:c.5099C= ENSP00000382432.2:p.Ser1700=
ENST00000587184.5:c.272C= ENSP00000466557.1:p.Ser91=
NM_000227.4:c.272C= NP_000218.3:p.Ser91=
NM_001127717.2:c.5099C= NP_001121189.2:p.Ser1700=
NM_001127718.2:c.272C= NP_001121190.2:p.Ser91=
NM_198129.2:c.5099C= NP_937762.2:p.Ser1700=
XM_011525978.1:c.5126C= XP_011524280.1:p.Ser1709=
XM_011525979.1:c.5117C= XP_011524281.1:p.Ser1706=
XM_011525980.1:c.5108C= XP_011524282.1:p.Ser1703=
XM_011525981.1:c.4994C= XP_011524283.1:p.Ser1665=
XM_011525982.1:c.5126C= XP_011524284.1:p.Ser1709=
XM_011525978.2:c.5126C= XP_011524280.1:p.Ser1709=
XM_011525979.2:c.5117C= XP_011524281.1:p.Ser1706=
XM_011525980.2:c.5108C= XP_011524282.1:p.Ser1703=
XM_011525981.2:c.4994C= XP_011524283.1:p.Ser1665=
XM_011525982.2:c.5126C= XP_011524284.1:p.Ser1709=
XM_017025743.1:c.2978C= XP_016881232.1:p.Ser993=
XM_017025744.1:c.668C= XP_016881233.1:p.Ser223=
XR_001753199.1:n.5367C=
NM_000227.5:c.272C= NP_000218.3:p.Ser91=
NM_001127717.3:c.5099C= NP_001121189.2:p.Ser1700=
NM_001127718.3:c.272C= NP_001121190.2:p.Ser91=
NM_198129.3:c.5099C= NP_937762.2:p.Ser1700=
NM_000227.6:c.272C= MANE Plus Clinical NP_000218.3:p.Ser91=
NM_001127717.4:c.5099C= NP_001121189.2:p.Ser1700=
NM_001127718.4:c.272C= NP_001121190.2:p.Ser91=
NM_198129.4:c.5099C= MANE Select NP_937762.2:p.Ser1700=