Canonical Allele Identifier: CA2641293871

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23876190-AAAAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876194_23876197del , CM000680.2:g.23876194_23876197del	GRCh38
NC_000018.9:g.21456158_21456161del , CM000680.1:g.21456158_21456161del	GRCh37
NC_000018.8:g.19710156_19710159del	NCBI36
NG_007853.2:g.191597_191600del

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.172-100_172-97del MANE Plus Clinical	ENSP00000269217.5:n.172-100_172-97del
ENST00000313654.14:c.4999-100_4999-97del MANE Select	ENSP00000324532.8:n.4999-100_4999-97del
ENST00000649721.1:c.1891-100_1891-97del	ENSP00000497885.1:n.1891-100_1891-97del
ENST00000269217.10:c.172-100_172-97del	ENSP00000269217.5:n.172-100_172-97del
ENST00000313654.13:c.4999-100_4999-97del	ENSP00000324532.8:n.4999-100_4999-97del
ENST00000399516.7:c.4999-100_4999-97del	ENSP00000382432.2:n.4999-100_4999-97del
ENST00000587184.5:c.172-100_172-97del	ENSP00000466557.1:n.172-100_172-97del
NM_000227.4:c.172-100_172-97del	NP_000218.3:n.172-100_172-97del
NM_001127717.2:c.4999-100_4999-97del	NP_001121189.2:n.4999-100_4999-97del
NM_001127718.2:c.172-100_172-97del	NP_001121190.2:n.172-100_172-97del
NM_198129.2:c.4999-100_4999-97del	NP_937762.2:n.4999-100_4999-97del
XM_011525978.1:c.5026-100_5026-97del	XP_011524280.1:n.5026-100_5026-97del
XM_011525979.1:c.5017-100_5017-97del	XP_011524281.1:n.5017-100_5017-97del
XM_011525980.1:c.5008-100_5008-97del	XP_011524282.1:n.5008-100_5008-97del
XM_011525981.1:c.4894-100_4894-97del	XP_011524283.1:n.4894-100_4894-97del
XM_011525982.1:c.5026-100_5026-97del	XP_011524284.1:n.5026-100_5026-97del
XM_011525978.2:c.5026-100_5026-97del	XP_011524280.1:n.5026-100_5026-97del
XM_011525979.2:c.5017-100_5017-97del	XP_011524281.1:n.5017-100_5017-97del
XM_011525980.2:c.5008-100_5008-97del	XP_011524282.1:n.5008-100_5008-97del
XM_011525981.2:c.4894-100_4894-97del	XP_011524283.1:n.4894-100_4894-97del
XM_011525982.2:c.5026-100_5026-97del	XP_011524284.1:n.5026-100_5026-97del
XM_017025743.1:c.2878-100_2878-97del	XP_016881232.1:n.2878-100_2878-97del
XM_017025744.1:c.568-100_568-97del	XP_016881233.1:n.568-100_568-97del
XR_001753199.1:n.5267-100_5267-97del
NM_000227.5:c.172-100_172-97del	NP_000218.3:n.172-100_172-97del
NM_001127717.3:c.4999-100_4999-97del	NP_001121189.2:n.4999-100_4999-97del
NM_001127718.3:c.172-100_172-97del	NP_001121190.2:n.172-100_172-97del
NM_198129.3:c.4999-100_4999-97del	NP_937762.2:n.4999-100_4999-97del
NM_000227.6:c.172-100_172-97del MANE Plus Clinical	NP_000218.3:n.172-100_172-97del
NM_001127717.4:c.4999-100_4999-97del	NP_001121189.2:n.4999-100_4999-97del
NM_001127718.4:c.172-100_172-97del	NP_001121190.2:n.172-100_172-97del
NM_198129.4:c.4999-100_4999-97del MANE Select	NP_937762.2:n.4999-100_4999-97del