Canonical Allele Identifier: CA503327954

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21456365A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876401A>C , CM000680.2:g.23876401A>C	GRCh38
NC_000018.9:g.21456365A>C , CM000680.1:g.21456365A>C	GRCh37
NC_000018.8:g.19710363A>C	NCBI36
NG_007853.2:g.191804A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.279A>C MANE Plus Clinical	ENSP00000269217.5:p.Ile93=
ENST00000313654.14:c.5106A>C MANE Select	ENSP00000324532.8:p.Ile1702=
ENST00000649721.1:c.1998A>C	ENSP00000497885.1:p.Ile666=
ENST00000269217.10:c.279A>C	ENSP00000269217.5:p.Ile93=
ENST00000313654.13:c.5106A>C	ENSP00000324532.8:p.Ile1702=
ENST00000399516.7:c.5106A>C	ENSP00000382432.2:p.Ile1702=
ENST00000587184.5:c.279A>C	ENSP00000466557.1:p.Ile93=
NM_000227.4:c.279A>C	NP_000218.3:p.Ile93=
NM_001127717.2:c.5106A>C	NP_001121189.2:p.Ile1702=
NM_001127718.2:c.279A>C	NP_001121190.2:p.Ile93=
NM_198129.2:c.5106A>C	NP_937762.2:p.Ile1702=
XM_011525978.1:c.5133A>C	XP_011524280.1:p.Ile1711=
XM_011525979.1:c.5124A>C	XP_011524281.1:p.Ile1708=
XM_011525980.1:c.5115A>C	XP_011524282.1:p.Ile1705=
XM_011525981.1:c.5001A>C	XP_011524283.1:p.Ile1667=
XM_011525982.1:c.5133A>C	XP_011524284.1:p.Ile1711=
XM_011525978.2:c.5133A>C	XP_011524280.1:p.Ile1711=
XM_011525979.2:c.5124A>C	XP_011524281.1:p.Ile1708=
XM_011525980.2:c.5115A>C	XP_011524282.1:p.Ile1705=
XM_011525981.2:c.5001A>C	XP_011524283.1:p.Ile1667=
XM_011525982.2:c.5133A>C	XP_011524284.1:p.Ile1711=
XM_017025743.1:c.2985A>C	XP_016881232.1:p.Ile995=
XM_017025744.1:c.675A>C	XP_016881233.1:p.Ile225=
XR_001753199.1:n.5374A>C
NM_000227.5:c.279A>C	NP_000218.3:p.Ile93=
NM_001127717.3:c.5106A>C	NP_001121189.2:p.Ile1702=
NM_001127718.3:c.279A>C	NP_001121190.2:p.Ile93=
NM_198129.3:c.5106A>C	NP_937762.2:p.Ile1702=
NM_000227.6:c.279A>C MANE Plus Clinical	NP_000218.3:p.Ile93=
NM_001127717.4:c.5106A>C	NP_001121189.2:p.Ile1702=
NM_001127718.4:c.279A>C	NP_001121190.2:p.Ile93=
NM_198129.4:c.5106A>C MANE Select	NP_937762.2:p.Ile1702=