Canonical Allele Identifier: CA2641292557

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23876271-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876271T>G , CM000680.2:g.23876271T>G	GRCh38
NC_000018.9:g.21456235T>G , CM000680.1:g.21456235T>G	GRCh37
NC_000018.8:g.19710233T>G	NCBI36
NG_007853.2:g.191674T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.172-23T>G MANE Plus Clinical	ENSP00000269217.5:n.172-23T>G
ENST00000313654.14:c.4999-23T>G MANE Select	ENSP00000324532.8:n.4999-23T>G
ENST00000649721.1:c.1891-23T>G	ENSP00000497885.1:n.1891-23T>G
ENST00000269217.10:c.172-23T>G	ENSP00000269217.5:n.172-23T>G
ENST00000313654.13:c.4999-23T>G	ENSP00000324532.8:n.4999-23T>G
ENST00000399516.7:c.4999-23T>G	ENSP00000382432.2:n.4999-23T>G
ENST00000587184.5:c.172-23T>G	ENSP00000466557.1:n.172-23T>G
NM_000227.4:c.172-23T>G	NP_000218.3:n.172-23T>G
NM_001127717.2:c.4999-23T>G	NP_001121189.2:n.4999-23T>G
NM_001127718.2:c.172-23T>G	NP_001121190.2:n.172-23T>G
NM_198129.2:c.4999-23T>G	NP_937762.2:n.4999-23T>G
XM_011525978.1:c.5026-23T>G	XP_011524280.1:n.5026-23T>G
XM_011525979.1:c.5017-23T>G	XP_011524281.1:n.5017-23T>G
XM_011525980.1:c.5008-23T>G	XP_011524282.1:n.5008-23T>G
XM_011525981.1:c.4894-23T>G	XP_011524283.1:n.4894-23T>G
XM_011525982.1:c.5026-23T>G	XP_011524284.1:n.5026-23T>G
XM_011525978.2:c.5026-23T>G	XP_011524280.1:n.5026-23T>G
XM_011525979.2:c.5017-23T>G	XP_011524281.1:n.5017-23T>G
XM_011525980.2:c.5008-23T>G	XP_011524282.1:n.5008-23T>G
XM_011525981.2:c.4894-23T>G	XP_011524283.1:n.4894-23T>G
XM_011525982.2:c.5026-23T>G	XP_011524284.1:n.5026-23T>G
XM_017025743.1:c.2878-23T>G	XP_016881232.1:n.2878-23T>G
XM_017025744.1:c.568-23T>G	XP_016881233.1:n.568-23T>G
XR_001753199.1:n.5267-23T>G
NM_000227.5:c.172-23T>G	NP_000218.3:n.172-23T>G
NM_001127717.3:c.4999-23T>G	NP_001121189.2:n.4999-23T>G
NM_001127718.3:c.172-23T>G	NP_001121190.2:n.172-23T>G
NM_198129.3:c.4999-23T>G	NP_937762.2:n.4999-23T>G
NM_000227.6:c.172-23T>G MANE Plus Clinical	NP_000218.3:n.172-23T>G
NM_001127717.4:c.4999-23T>G	NP_001121189.2:n.4999-23T>G
NM_001127718.4:c.172-23T>G	NP_001121190.2:n.172-23T>G
NM_198129.4:c.4999-23T>G MANE Select	NP_937762.2:n.4999-23T>G