Canonical Allele Identifier: CA503522777

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21529997C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950033C>T , CM000680.2:g.23950033C>T	GRCh38
NC_000018.9:g.21529997C>T , CM000680.1:g.21529997C>T	GRCh37
NC_000018.8:g.19783995C>T	NCBI36
NG_007853.2:g.265436C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4689C>T MANE Plus Clinical	ENSP00000269217.5:p.His1563=
ENST00000313654.14:c.9516C>T MANE Select	ENSP00000324532.8:p.His3172=
ENST00000649721.1:c.6111C>T	ENSP00000497885.1:p.His2037=
ENST00000269217.10:c.4689C>T	ENSP00000269217.5:p.His1563=
ENST00000313654.13:c.9516C>T	ENSP00000324532.8:p.His3172=
ENST00000399516.7:c.9348C>T	ENSP00000382432.2:p.His3116=
ENST00000587184.5:c.4521C>T	ENSP00000466557.1:p.His1507=
ENST00000588004.1:c.37C>T
ENST00000588770.5:n.4094C>T
NM_000227.4:c.4689C>T	NP_000218.3:p.His1563=
NM_001127717.2:c.9348C>T	NP_001121189.2:p.His3116=
NM_001127718.2:c.4521C>T	NP_001121190.2:p.His1507=
NM_198129.2:c.9516C>T	NP_937762.2:p.His3172=
XM_011525978.1:c.9543C>T	XP_011524280.1:p.His3181=
XM_011525979.1:c.9534C>T	XP_011524281.1:p.His3178=
XM_011525980.1:c.9525C>T	XP_011524282.1:p.His3175=
XM_011525981.1:c.9411C>T	XP_011524283.1:p.His3137=
XM_011525982.1:c.9246C>T	XP_011524284.1:p.His3082=
XM_011525978.2:c.9543C>T	XP_011524280.1:p.His3181=
XM_011525979.2:c.9534C>T	XP_011524281.1:p.His3178=
XM_011525980.2:c.9525C>T	XP_011524282.1:p.His3175=
XM_011525981.2:c.9411C>T	XP_011524283.1:p.His3137=
XM_011525982.2:c.9246C>T	XP_011524284.1:p.His3082=
XM_017025743.1:c.7395C>T	XP_016881232.1:p.His2465=
XM_017025744.1:c.5085C>T	XP_016881233.1:p.His1695=
XR_001753199.1:n.9784C>T
NM_000227.5:c.4689C>T	NP_000218.3:p.His1563=
NM_001127717.3:c.9348C>T	NP_001121189.2:p.His3116=
NM_001127718.3:c.4521C>T	NP_001121190.2:p.His1507=
NM_198129.3:c.9516C>T	NP_937762.2:p.His3172=
NM_000227.6:c.4689C>T MANE Plus Clinical	NP_000218.3:p.His1563=
NM_001127717.4:c.9348C>T	NP_001121189.2:p.His3116=
NM_001127718.4:c.4521C>T	NP_001121190.2:p.His1507=
NM_198129.4:c.9516C>T MANE Select	NP_937762.2:p.His3172=