Canonical Allele Identifier: CA402059252

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495333C>G (hg19) ; chr18:g.23915369C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915369C>G , CM000680.2:g.23915369C>G	GRCh38
NC_000018.9:g.21495333C>G , CM000680.1:g.21495333C>G	GRCh37
NC_000018.8:g.19749331C>G	NCBI36
NG_007853.2:g.230772C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2898C>G MANE Plus Clinical	ENSP00000269217.5:p.Tyr966Ter
ENST00000313654.14:c.7725C>G MANE Select	ENSP00000324532.8:p.Tyr2575Ter
ENST00000649721.1:c.4320C>G	ENSP00000497885.1:p.Tyr1440Ter
ENST00000269217.10:c.2898C>G	ENSP00000269217.5:p.Tyr966Ter
ENST00000313654.13:c.7725C>G	ENSP00000324532.8:p.Tyr2575Ter
ENST00000399516.7:c.7557C>G	ENSP00000382432.2:p.Tyr2519Ter
ENST00000586751.5:c.2503C>G
ENST00000587184.5:c.2730C>G	ENSP00000466557.1:p.Tyr910Ter
ENST00000588770.5:n.2303C>G
NM_000227.4:c.2898C>G	NP_000218.3:p.Tyr966Ter
NM_001127717.2:c.7557C>G	NP_001121189.2:p.Tyr2519Ter
NM_001127718.2:c.2730C>G	NP_001121190.2:p.Tyr910Ter
NM_198129.2:c.7725C>G	NP_937762.2:p.Tyr2575Ter
XM_011525978.1:c.7752C>G	XP_011524280.1:p.Tyr2584Ter
XM_011525979.1:c.7743C>G	XP_011524281.1:p.Tyr2581Ter
XM_011525980.1:c.7734C>G	XP_011524282.1:p.Tyr2578Ter
XM_011525981.1:c.7620C>G	XP_011524283.1:p.Tyr2540Ter
XM_011525982.1:c.7455C>G	XP_011524284.1:p.Tyr2485Ter
XM_011525978.2:c.7752C>G	XP_011524280.1:p.Tyr2584Ter
XM_011525979.2:c.7743C>G	XP_011524281.1:p.Tyr2581Ter
XM_011525980.2:c.7734C>G	XP_011524282.1:p.Tyr2578Ter
XM_011525981.2:c.7620C>G	XP_011524283.1:p.Tyr2540Ter
XM_011525982.2:c.7455C>G	XP_011524284.1:p.Tyr2485Ter
XM_017025743.1:c.5604C>G	XP_016881232.1:p.Tyr1868Ter
XM_017025744.1:c.3294C>G	XP_016881233.1:p.Tyr1098Ter
XR_001753199.1:n.7993C>G
NM_000227.5:c.2898C>G	NP_000218.3:p.Tyr966Ter
NM_001127717.3:c.7557C>G	NP_001121189.2:p.Tyr2519Ter
NM_001127718.3:c.2730C>G	NP_001121190.2:p.Tyr910Ter
NM_198129.3:c.7725C>G	NP_937762.2:p.Tyr2575Ter
NM_000227.6:c.2898C>G MANE Plus Clinical	NP_000218.3:p.Tyr966Ter
NM_001127717.4:c.7557C>G	NP_001121189.2:p.Tyr2519Ter
NM_001127718.4:c.2730C>G	NP_001121190.2:p.Tyr910Ter
NM_198129.4:c.7725C>G MANE Select	NP_937762.2:p.Tyr2575Ter