Canonical Allele Identifier: CA402044843

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.23876247_23876248del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876247_23876248del , CM000680.2:g.23876247_23876248del	GRCh38
NC_000018.9:g.21456211_21456212del , CM000680.1:g.21456211_21456212del	GRCh37
NC_000018.8:g.19710209_19710210del	NCBI36
NG_007853.2:g.191650_191651del

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.172-47_172-46del MANE Plus Clinical	ENSP00000269217.5:n.172-47_172-46del
ENST00000313654.14:c.4999-47_4999-46del MANE Select	ENSP00000324532.8:n.4999-47_4999-46del
ENST00000649721.1:c.1891-47_1891-46del	ENSP00000497885.1:n.1891-47_1891-46del
ENST00000269217.10:c.172-47_172-46del	ENSP00000269217.5:n.172-47_172-46del
ENST00000313654.13:c.4999-47_4999-46del	ENSP00000324532.8:n.4999-47_4999-46del
ENST00000399516.7:c.4999-47_4999-46del	ENSP00000382432.2:n.4999-47_4999-46del
ENST00000587184.5:c.172-47_172-46del	ENSP00000466557.1:n.172-47_172-46del
NM_000227.4:c.172-47_172-46del	NP_000218.3:n.172-47_172-46del
NM_001127717.2:c.4999-47_4999-46del	NP_001121189.2:n.4999-47_4999-46del
NM_001127718.2:c.172-47_172-46del	NP_001121190.2:n.172-47_172-46del
NM_198129.2:c.4999-47_4999-46del	NP_937762.2:n.4999-47_4999-46del
XM_011525978.1:c.5026-47_5026-46del	XP_011524280.1:n.5026-47_5026-46del
XM_011525979.1:c.5017-47_5017-46del	XP_011524281.1:n.5017-47_5017-46del
XM_011525980.1:c.5008-47_5008-46del	XP_011524282.1:n.5008-47_5008-46del
XM_011525981.1:c.4894-47_4894-46del	XP_011524283.1:n.4894-47_4894-46del
XM_011525982.1:c.5026-47_5026-46del	XP_011524284.1:n.5026-47_5026-46del
XM_011525978.2:c.5026-47_5026-46del	XP_011524280.1:n.5026-47_5026-46del
XM_011525979.2:c.5017-47_5017-46del	XP_011524281.1:n.5017-47_5017-46del
XM_011525980.2:c.5008-47_5008-46del	XP_011524282.1:n.5008-47_5008-46del
XM_011525981.2:c.4894-47_4894-46del	XP_011524283.1:n.4894-47_4894-46del
XM_011525982.2:c.5026-47_5026-46del	XP_011524284.1:n.5026-47_5026-46del
XM_017025743.1:c.2878-47_2878-46del	XP_016881232.1:n.2878-47_2878-46del
XM_017025744.1:c.568-47_568-46del	XP_016881233.1:n.568-47_568-46del
XR_001753199.1:n.5267-47_5267-46del
NM_000227.5:c.172-47_172-46del	NP_000218.3:n.172-47_172-46del
NM_001127717.3:c.4999-47_4999-46del	NP_001121189.2:n.4999-47_4999-46del
NM_001127718.3:c.172-47_172-46del	NP_001121190.2:n.172-47_172-46del
NM_198129.3:c.4999-47_4999-46del	NP_937762.2:n.4999-47_4999-46del
NM_000227.6:c.172-47_172-46del MANE Plus Clinical	NP_000218.3:n.172-47_172-46del
NM_001127717.4:c.4999-47_4999-46del	NP_001121189.2:n.4999-47_4999-46del
NM_001127718.4:c.172-47_172-46del	NP_001121190.2:n.172-47_172-46del
NM_198129.4:c.4999-47_4999-46del MANE Select	NP_937762.2:n.4999-47_4999-46del