Canonical Allele Identifier: CA2290329056
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23915517A= , CM000680.2:g.23915517A= GRCh38
NC_000018.9:g.21495481A= , CM000680.1:g.21495481A= GRCh37
NC_000018.8:g.19749479A= NCBI36
NG_007853.2:g.230920A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.2951+95A= MANE Plus Clinical ENSP00000269217.5:n.2951+95A=
ENST00000313654.14:c.7778+95A= MANE Select ENSP00000324532.8:n.7778+95A=
ENST00000649721.1:c.4373+95A= ENSP00000497885.1:n.4373+95A=
ENST00000269217.10:c.2951+95A= ENSP00000269217.5:n.2951+95A=
ENST00000313654.13:c.7778+95A= ENSP00000324532.8:n.7778+95A=
ENST00000399516.7:c.7610+95A= ENSP00000382432.2:n.7610+95A=
ENST00000586751.5:c.2556+95A=
ENST00000587184.5:c.2783+95A= ENSP00000466557.1:n.2783+95A=
ENST00000588770.5:n.2356+95A=
NM_000227.4:c.2951+95A= NP_000218.3:n.2951+95A=
NM_001127717.2:c.7610+95A= NP_001121189.2:n.7610+95A=
NM_001127718.2:c.2783+95A= NP_001121190.2:n.2783+95A=
NM_198129.2:c.7778+95A= NP_937762.2:n.7778+95A=
XM_011525978.1:c.7805+95A= XP_011524280.1:n.7805+95A=
XM_011525979.1:c.7796+95A= XP_011524281.1:n.7796+95A=
XM_011525980.1:c.7787+95A= XP_011524282.1:n.7787+95A=
XM_011525981.1:c.7673+95A= XP_011524283.1:n.7673+95A=
XM_011525982.1:c.7508+95A= XP_011524284.1:n.7508+95A=
XM_011525978.2:c.7805+95A= XP_011524280.1:n.7805+95A=
XM_011525979.2:c.7796+95A= XP_011524281.1:n.7796+95A=
XM_011525980.2:c.7787+95A= XP_011524282.1:n.7787+95A=
XM_011525981.2:c.7673+95A= XP_011524283.1:n.7673+95A=
XM_011525982.2:c.7508+95A= XP_011524284.1:n.7508+95A=
XM_017025743.1:c.5657+95A= XP_016881232.1:n.5657+95A=
XM_017025744.1:c.3347+95A= XP_016881233.1:n.3347+95A=
XR_001753199.1:n.8046+95A=
NM_000227.5:c.2951+95A= NP_000218.3:n.2951+95A=
NM_001127717.3:c.7610+95A= NP_001121189.2:n.7610+95A=
NM_001127718.3:c.2783+95A= NP_001121190.2:n.2783+95A=
NM_198129.3:c.7778+95A= NP_937762.2:n.7778+95A=
NM_000227.6:c.2951+95A= MANE Plus Clinical NP_000218.3:n.2951+95A=
NM_001127717.4:c.7610+95A= NP_001121189.2:n.7610+95A=
NM_001127718.4:c.2783+95A= NP_001121190.2:n.2783+95A=
NM_198129.4:c.7778+95A= MANE Select NP_937762.2:n.7778+95A=