Canonical Allele Identifier: CA2641297187

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23927977-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23927977C>G , CM000680.2:g.23927977C>G	GRCh38
NC_000018.9:g.21507941C>G , CM000680.1:g.21507941C>G	GRCh37
NC_000018.8:g.19761939C>G	NCBI36
NG_007853.2:g.243380C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3351-146C>G MANE Plus Clinical	ENSP00000269217.5:n.3351-146C>G
ENST00000313654.14:c.8178-146C>G MANE Select	ENSP00000324532.8:n.8178-146C>G
ENST00000649721.1:c.4773-146C>G	ENSP00000497885.1:n.4773-146C>G
ENST00000269217.10:c.3351-146C>G	ENSP00000269217.5:n.3351-146C>G
ENST00000313654.13:c.8178-146C>G	ENSP00000324532.8:n.8178-146C>G
ENST00000399516.7:c.8010-146C>G	ENSP00000382432.2:n.8010-146C>G
ENST00000586751.5:c.2956-146C>G
ENST00000587184.5:c.3183-146C>G	ENSP00000466557.1:n.3183-146C>G
ENST00000588770.5:n.2756-146C>G
NM_000227.4:c.3351-146C>G	NP_000218.3:n.3351-146C>G
NM_001127717.2:c.8010-146C>G	NP_001121189.2:n.8010-146C>G
NM_001127718.2:c.3183-146C>G	NP_001121190.2:n.3183-146C>G
NM_198129.2:c.8178-146C>G	NP_937762.2:n.8178-146C>G
XM_011525978.1:c.8205-146C>G	XP_011524280.1:n.8205-146C>G
XM_011525979.1:c.8196-146C>G	XP_011524281.1:n.8196-146C>G
XM_011525980.1:c.8187-146C>G	XP_011524282.1:n.8187-146C>G
XM_011525981.1:c.8073-146C>G	XP_011524283.1:n.8073-146C>G
XM_011525982.1:c.7908-146C>G	XP_011524284.1:n.7908-146C>G
XM_011525978.2:c.8205-146C>G	XP_011524280.1:n.8205-146C>G
XM_011525979.2:c.8196-146C>G	XP_011524281.1:n.8196-146C>G
XM_011525980.2:c.8187-146C>G	XP_011524282.1:n.8187-146C>G
XM_011525981.2:c.8073-146C>G	XP_011524283.1:n.8073-146C>G
XM_011525982.2:c.7908-146C>G	XP_011524284.1:n.7908-146C>G
XM_017025743.1:c.6057-146C>G	XP_016881232.1:n.6057-146C>G
XM_017025744.1:c.3747-146C>G	XP_016881233.1:n.3747-146C>G
XR_001753199.1:n.8446-146C>G
NM_000227.5:c.3351-146C>G	NP_000218.3:n.3351-146C>G
NM_001127717.3:c.8010-146C>G	NP_001121189.2:n.8010-146C>G
NM_001127718.3:c.3183-146C>G	NP_001121190.2:n.3183-146C>G
NM_198129.3:c.8178-146C>G	NP_937762.2:n.8178-146C>G
NM_000227.6:c.3351-146C>G MANE Plus Clinical	NP_000218.3:n.3351-146C>G
NM_001127717.4:c.8010-146C>G	NP_001121189.2:n.8010-146C>G
NM_001127718.4:c.3183-146C>G	NP_001121190.2:n.3183-146C>G
NM_198129.4:c.8178-146C>G MANE Select	NP_937762.2:n.8178-146C>G