Canonical Allele Identifier: CA503327850

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21456293C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876329C>T , CM000680.2:g.23876329C>T	GRCh38
NC_000018.9:g.21456293C>T , CM000680.1:g.21456293C>T	GRCh37
NC_000018.8:g.19710291C>T	NCBI36
NG_007853.2:g.191732C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.207C>T MANE Plus Clinical	ENSP00000269217.5:p.Gly69=
ENST00000313654.14:c.5034C>T MANE Select	ENSP00000324532.8:p.Gly1678=
ENST00000649721.1:c.1926C>T	ENSP00000497885.1:p.Gly642=
ENST00000269217.10:c.207C>T	ENSP00000269217.5:p.Gly69=
ENST00000313654.13:c.5034C>T	ENSP00000324532.8:p.Gly1678=
ENST00000399516.7:c.5034C>T	ENSP00000382432.2:p.Gly1678=
ENST00000587184.5:c.207C>T	ENSP00000466557.1:p.Gly69=
NM_000227.4:c.207C>T	NP_000218.3:p.Gly69=
NM_001127717.2:c.5034C>T	NP_001121189.2:p.Gly1678=
NM_001127718.2:c.207C>T	NP_001121190.2:p.Gly69=
NM_198129.2:c.5034C>T	NP_937762.2:p.Gly1678=
XM_011525978.1:c.5061C>T	XP_011524280.1:p.Gly1687=
XM_011525979.1:c.5052C>T	XP_011524281.1:p.Gly1684=
XM_011525980.1:c.5043C>T	XP_011524282.1:p.Gly1681=
XM_011525981.1:c.4929C>T	XP_011524283.1:p.Gly1643=
XM_011525982.1:c.5061C>T	XP_011524284.1:p.Gly1687=
XM_011525978.2:c.5061C>T	XP_011524280.1:p.Gly1687=
XM_011525979.2:c.5052C>T	XP_011524281.1:p.Gly1684=
XM_011525980.2:c.5043C>T	XP_011524282.1:p.Gly1681=
XM_011525981.2:c.4929C>T	XP_011524283.1:p.Gly1643=
XM_011525982.2:c.5061C>T	XP_011524284.1:p.Gly1687=
XM_017025743.1:c.2913C>T	XP_016881232.1:p.Gly971=
XM_017025744.1:c.603C>T	XP_016881233.1:p.Gly201=
XR_001753199.1:n.5302C>T
NM_000227.5:c.207C>T	NP_000218.3:p.Gly69=
NM_001127717.3:c.5034C>T	NP_001121189.2:p.Gly1678=
NM_001127718.3:c.207C>T	NP_001121190.2:p.Gly69=
NM_198129.3:c.5034C>T	NP_937762.2:p.Gly1678=
NM_000227.6:c.207C>T MANE Plus Clinical	NP_000218.3:p.Gly69=
NM_001127717.4:c.5034C>T	NP_001121189.2:p.Gly1678=
NM_001127718.4:c.207C>T	NP_001121190.2:p.Gly69=
NM_198129.4:c.5034C>T MANE Select	NP_937762.2:p.Gly1678=