Canonical Allele Identifier: CA2290299494
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23845887_23845888delinsGT , CM000680.2:g.23845887_23845888delinsGT GRCh38
NC_000018.9:g.21425851_21425852delinsGT , CM000680.1:g.21425851_21425852delinsGT GRCh37
NC_000018.8:g.19679849_19679850delinsGT NCBI36
NG_007853.2:g.161290_161291delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000313654.14:c.3720-410_3720-409delinsGT MANE Select ENSP00000324532.8:n.3720-410_3720-409deli...
ENST00000649721.1:c.612-410_612-409delinsGT ENSP00000497885.1:n.612-410_612-409delins...
ENST00000313654.13:c.3720-410_3720-409delinsGT ENSP00000324532.8:n.3720-410_3720-409deli...
ENST00000399516.7:c.3720-410_3720-409delinsGT ENSP00000382432.2:n.3720-410_3720-409deli...
NM_001127717.2:c.3720-410_3720-409delinsGT NP_001121189.2:n.3720-410_3720-409delinsG...
NM_198129.2:c.3720-410_3720-409delinsGT NP_937762.2:n.3720-410_3720-409delinsGT
XM_011525978.1:c.3747-410_3747-409delinsGT XP_011524280.1:n.3747-410_3747-409delinsG...
XM_011525979.1:c.3738-410_3738-409delinsGT XP_011524281.1:n.3738-410_3738-409delinsG...
XM_011525980.1:c.3729-410_3729-409delinsGT XP_011524282.1:n.3729-410_3729-409delinsG...
XM_011525981.1:c.3615-410_3615-409delinsGT XP_011524283.1:n.3615-410_3615-409delinsG...
XM_011525982.1:c.3747-410_3747-409delinsGT XP_011524284.1:n.3747-410_3747-409delinsG...
XM_011525978.2:c.3747-410_3747-409delinsGT XP_011524280.1:n.3747-410_3747-409delinsG...
XM_011525979.2:c.3738-410_3738-409delinsGT XP_011524281.1:n.3738-410_3738-409delinsG...
XM_011525980.2:c.3729-410_3729-409delinsGT XP_011524282.1:n.3729-410_3729-409delinsG...
XM_011525981.2:c.3615-410_3615-409delinsGT XP_011524283.1:n.3615-410_3615-409delinsG...
XM_011525982.2:c.3747-410_3747-409delinsGT XP_011524284.1:n.3747-410_3747-409delinsG...
XM_017025743.1:c.1599-410_1599-409delinsGT XP_016881232.1:n.1599-410_1599-409delinsG...
XM_017025744.1:c.-905-410_-905-409delinsGT XP_016881233.1:n.-905-410_-905-409delinsG...
XR_001753199.1:n.3988-410_3988-409delinsGT
NM_001127717.3:c.3720-410_3720-409delinsGT NP_001121189.2:n.3720-410_3720-409delinsG...
NM_198129.3:c.3720-410_3720-409delinsGT NP_937762.2:n.3720-410_3720-409delinsGT
NM_001127717.4:c.3720-410_3720-409delinsGT NP_001121189.2:n.3720-410_3720-409delinsG...
NM_198129.4:c.3720-410_3720-409delinsGT MANE Select NP_937762.2:n.3720-410_3720-409delinsGT