Canonical Allele Identifier: CA777750276

Gene: LAMA3

Linked Data

• dbSNP Id: rs1447001191
• MyVariant Identifiers: chr18:g.21456242_21456245del (hg19) ; chr18:g.23876278_23876281del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876282_23876285del , CM000680.2:g.23876282_23876285del	GRCh38
NC_000018.9:g.21456246_21456249del , CM000680.1:g.21456246_21456249del	GRCh37
NC_000018.8:g.19710244_19710247del	NCBI36
NG_007853.2:g.191685_191688del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.172-12_172-9del MANE Plus Clinical	ENSP00000269217.5:n.172-12_172-9del
ENST00000313654.14:c.4999-12_4999-9del MANE Select	ENSP00000324532.8:n.4999-12_4999-9del
ENST00000649721.1:c.1891-12_1891-9del	ENSP00000497885.1:n.1891-12_1891-9del
ENST00000269217.10:c.172-12_172-9del	ENSP00000269217.5:n.172-12_172-9del
ENST00000313654.13:c.4999-12_4999-9del	ENSP00000324532.8:n.4999-12_4999-9del
ENST00000399516.7:c.4999-12_4999-9del	ENSP00000382432.2:n.4999-12_4999-9del
ENST00000587184.5:c.172-12_172-9del	ENSP00000466557.1:n.172-12_172-9del
NM_000227.4:c.172-12_172-9del	NP_000218.3:n.172-12_172-9del
NM_001127717.2:c.4999-12_4999-9del	NP_001121189.2:n.4999-12_4999-9del
NM_001127718.2:c.172-12_172-9del	NP_001121190.2:n.172-12_172-9del
NM_198129.2:c.4999-12_4999-9del	NP_937762.2:n.4999-12_4999-9del
XM_011525978.1:c.5026-12_5026-9del	XP_011524280.1:n.5026-12_5026-9del
XM_011525979.1:c.5017-12_5017-9del	XP_011524281.1:n.5017-12_5017-9del
XM_011525980.1:c.5008-12_5008-9del	XP_011524282.1:n.5008-12_5008-9del
XM_011525981.1:c.4894-12_4894-9del	XP_011524283.1:n.4894-12_4894-9del
XM_011525982.1:c.5026-12_5026-9del	XP_011524284.1:n.5026-12_5026-9del
XM_011525978.2:c.5026-12_5026-9del	XP_011524280.1:n.5026-12_5026-9del
XM_011525979.2:c.5017-12_5017-9del	XP_011524281.1:n.5017-12_5017-9del
XM_011525980.2:c.5008-12_5008-9del	XP_011524282.1:n.5008-12_5008-9del
XM_011525981.2:c.4894-12_4894-9del	XP_011524283.1:n.4894-12_4894-9del
XM_011525982.2:c.5026-12_5026-9del	XP_011524284.1:n.5026-12_5026-9del
XM_017025743.1:c.2878-12_2878-9del	XP_016881232.1:n.2878-12_2878-9del
XM_017025744.1:c.568-12_568-9del	XP_016881233.1:n.568-12_568-9del
XR_001753199.1:n.5267-12_5267-9del
NM_000227.5:c.172-12_172-9del	NP_000218.3:n.172-12_172-9del
NM_001127717.3:c.4999-12_4999-9del	NP_001121189.2:n.4999-12_4999-9del
NM_001127718.3:c.172-12_172-9del	NP_001121190.2:n.172-12_172-9del
NM_198129.3:c.4999-12_4999-9del	NP_937762.2:n.4999-12_4999-9del
NM_000227.6:c.172-12_172-9del MANE Plus Clinical	NP_000218.3:n.172-12_172-9del
NM_001127717.4:c.4999-12_4999-9del	NP_001121189.2:n.4999-12_4999-9del
NM_001127718.4:c.172-12_172-9del	NP_001121190.2:n.172-12_172-9del
NM_198129.4:c.4999-12_4999-9del MANE Select	NP_937762.2:n.4999-12_4999-9del