Canonical Allele Identifier: CA402045079

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21456364T>A (hg19) ; chr18:g.23876400T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876400T>A , CM000680.2:g.23876400T>A	GRCh38
NC_000018.9:g.21456364T>A , CM000680.1:g.21456364T>A	GRCh37
NC_000018.8:g.19710362T>A	NCBI36
NG_007853.2:g.191803T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.278T>A MANE Plus Clinical	ENSP00000269217.5:p.Ile93Lys
ENST00000313654.14:c.5105T>A MANE Select	ENSP00000324532.8:p.Ile1702Lys
ENST00000649721.1:c.1997T>A	ENSP00000497885.1:p.Ile666Lys
ENST00000269217.10:c.278T>A	ENSP00000269217.5:p.Ile93Lys
ENST00000313654.13:c.5105T>A	ENSP00000324532.8:p.Ile1702Lys
ENST00000399516.7:c.5105T>A	ENSP00000382432.2:p.Ile1702Lys
ENST00000587184.5:c.278T>A	ENSP00000466557.1:p.Ile93Lys
NM_000227.4:c.278T>A	NP_000218.3:p.Ile93Lys
NM_001127717.2:c.5105T>A	NP_001121189.2:p.Ile1702Lys
NM_001127718.2:c.278T>A	NP_001121190.2:p.Ile93Lys
NM_198129.2:c.5105T>A	NP_937762.2:p.Ile1702Lys
XM_011525978.1:c.5132T>A	XP_011524280.1:p.Ile1711Lys
XM_011525979.1:c.5123T>A	XP_011524281.1:p.Ile1708Lys
XM_011525980.1:c.5114T>A	XP_011524282.1:p.Ile1705Lys
XM_011525981.1:c.5000T>A	XP_011524283.1:p.Ile1667Lys
XM_011525982.1:c.5132T>A	XP_011524284.1:p.Ile1711Lys
XM_011525978.2:c.5132T>A	XP_011524280.1:p.Ile1711Lys
XM_011525979.2:c.5123T>A	XP_011524281.1:p.Ile1708Lys
XM_011525980.2:c.5114T>A	XP_011524282.1:p.Ile1705Lys
XM_011525981.2:c.5000T>A	XP_011524283.1:p.Ile1667Lys
XM_011525982.2:c.5132T>A	XP_011524284.1:p.Ile1711Lys
XM_017025743.1:c.2984T>A	XP_016881232.1:p.Ile995Lys
XM_017025744.1:c.674T>A	XP_016881233.1:p.Ile225Lys
XR_001753199.1:n.5373T>A
NM_000227.5:c.278T>A	NP_000218.3:p.Ile93Lys
NM_001127717.3:c.5105T>A	NP_001121189.2:p.Ile1702Lys
NM_001127718.3:c.278T>A	NP_001121190.2:p.Ile93Lys
NM_198129.3:c.5105T>A	NP_937762.2:p.Ile1702Lys
NM_000227.6:c.278T>A MANE Plus Clinical	NP_000218.3:p.Ile93Lys
NM_001127717.4:c.5105T>A	NP_001121189.2:p.Ile1702Lys
NM_001127718.4:c.278T>A	NP_001121190.2:p.Ile93Lys
NM_198129.4:c.5105T>A MANE Select	NP_937762.2:p.Ile1702Lys