Canonical Allele Identifier: CA503327839

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21456287T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876323T>C , CM000680.2:g.23876323T>C	GRCh38
NC_000018.9:g.21456287T>C , CM000680.1:g.21456287T>C	GRCh37
NC_000018.8:g.19710285T>C	NCBI36
NG_007853.2:g.191726T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.201T>C MANE Plus Clinical	ENSP00000269217.5:p.His67=
ENST00000313654.14:c.5028T>C MANE Select	ENSP00000324532.8:p.His1676=
ENST00000649721.1:c.1920T>C	ENSP00000497885.1:p.His640=
ENST00000269217.10:c.201T>C	ENSP00000269217.5:p.His67=
ENST00000313654.13:c.5028T>C	ENSP00000324532.8:p.His1676=
ENST00000399516.7:c.5028T>C	ENSP00000382432.2:p.His1676=
ENST00000587184.5:c.201T>C	ENSP00000466557.1:p.His67=
NM_000227.4:c.201T>C	NP_000218.3:p.His67=
NM_001127717.2:c.5028T>C	NP_001121189.2:p.His1676=
NM_001127718.2:c.201T>C	NP_001121190.2:p.His67=
NM_198129.2:c.5028T>C	NP_937762.2:p.His1676=
XM_011525978.1:c.5055T>C	XP_011524280.1:p.His1685=
XM_011525979.1:c.5046T>C	XP_011524281.1:p.His1682=
XM_011525980.1:c.5037T>C	XP_011524282.1:p.His1679=
XM_011525981.1:c.4923T>C	XP_011524283.1:p.His1641=
XM_011525982.1:c.5055T>C	XP_011524284.1:p.His1685=
XM_011525978.2:c.5055T>C	XP_011524280.1:p.His1685=
XM_011525979.2:c.5046T>C	XP_011524281.1:p.His1682=
XM_011525980.2:c.5037T>C	XP_011524282.1:p.His1679=
XM_011525981.2:c.4923T>C	XP_011524283.1:p.His1641=
XM_011525982.2:c.5055T>C	XP_011524284.1:p.His1685=
XM_017025743.1:c.2907T>C	XP_016881232.1:p.His969=
XM_017025744.1:c.597T>C	XP_016881233.1:p.His199=
XR_001753199.1:n.5296T>C
NM_000227.5:c.201T>C	NP_000218.3:p.His67=
NM_001127717.3:c.5028T>C	NP_001121189.2:p.His1676=
NM_001127718.3:c.201T>C	NP_001121190.2:p.His67=
NM_198129.3:c.5028T>C	NP_937762.2:p.His1676=
NM_000227.6:c.201T>C MANE Plus Clinical	NP_000218.3:p.His67=
NM_001127717.4:c.5028T>C	NP_001121189.2:p.His1676=
NM_001127718.4:c.201T>C	NP_001121190.2:p.His67=
NM_198129.4:c.5028T>C MANE Select	NP_937762.2:p.His1676=