Canonical Allele Identifier: CA2734663204
Gene: LAMA3 HGNC NCBI

Linked Data

dbSNP Id: rs2145374879

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928507_23928510del , CM000680.2:g.23928507_23928510del GRCh38
NC_000018.9:g.21508471_21508474del , CM000680.1:g.21508471_21508474del GRCh37
NC_000018.8:g.19762469_19762472del NCBI36
NG_007853.2:g.243910_243913del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.3469-118_3469-115del MANE Plus Clinical ENSP00000269217.5:n.3469-118_3469-115del
ENST00000313654.14:c.8296-118_8296-115del MANE Select ENSP00000324532.8:n.8296-118_8296-115del
ENST00000649721.1:c.4891-118_4891-115del ENSP00000497885.1:n.4891-118_4891-115del
ENST00000269217.10:c.3469-118_3469-115del ENSP00000269217.5:n.3469-118_3469-115del
ENST00000313654.13:c.8296-118_8296-115del ENSP00000324532.8:n.8296-118_8296-115del
ENST00000399516.7:c.8128-118_8128-115del ENSP00000382432.2:n.8128-118_8128-115del
ENST00000586751.5:c.3074-118_3074-115del
ENST00000587184.5:c.3301-118_3301-115del ENSP00000466557.1:n.3301-118_3301-115del
ENST00000588770.5:n.2874-118_2874-115del
NM_000227.4:c.3469-118_3469-115del NP_000218.3:n.3469-118_3469-115del
NM_001127717.2:c.8128-118_8128-115del NP_001121189.2:n.8128-118_8128-115del
NM_001127718.2:c.3301-118_3301-115del NP_001121190.2:n.3301-118_3301-115del
NM_198129.2:c.8296-118_8296-115del NP_937762.2:n.8296-118_8296-115del
XM_011525978.1:c.8323-118_8323-115del XP_011524280.1:n.8323-118_8323-115del
XM_011525979.1:c.8314-118_8314-115del XP_011524281.1:n.8314-118_8314-115del
XM_011525980.1:c.8305-118_8305-115del XP_011524282.1:n.8305-118_8305-115del
XM_011525981.1:c.8191-118_8191-115del XP_011524283.1:n.8191-118_8191-115del
XM_011525982.1:c.8026-118_8026-115del XP_011524284.1:n.8026-118_8026-115del
XM_011525978.2:c.8323-118_8323-115del XP_011524280.1:n.8323-118_8323-115del
XM_011525979.2:c.8314-118_8314-115del XP_011524281.1:n.8314-118_8314-115del
XM_011525980.2:c.8305-118_8305-115del XP_011524282.1:n.8305-118_8305-115del
XM_011525981.2:c.8191-118_8191-115del XP_011524283.1:n.8191-118_8191-115del
XM_011525982.2:c.8026-118_8026-115del XP_011524284.1:n.8026-118_8026-115del
XM_017025743.1:c.6175-118_6175-115del XP_016881232.1:n.6175-118_6175-115del
XM_017025744.1:c.3865-118_3865-115del XP_016881233.1:n.3865-118_3865-115del
XR_001753199.1:n.8564-118_8564-115del
NM_000227.5:c.3469-118_3469-115del NP_000218.3:n.3469-118_3469-115del
NM_001127717.3:c.8128-118_8128-115del NP_001121189.2:n.8128-118_8128-115del
NM_001127718.3:c.3301-118_3301-115del NP_001121190.2:n.3301-118_3301-115del
NM_198129.3:c.8296-118_8296-115del NP_937762.2:n.8296-118_8296-115del
NM_000227.6:c.3469-118_3469-115del MANE Plus Clinical NP_000218.3:n.3469-118_3469-115del
NM_001127717.4:c.8128-118_8128-115del NP_001121189.2:n.8128-118_8128-115del
NM_001127718.4:c.3301-118_3301-115del NP_001121190.2:n.3301-118_3301-115del
NM_198129.4:c.8296-118_8296-115del MANE Select NP_937762.2:n.8296-118_8296-115del