Canonical Allele Identifier: CA2290322254

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898994A= , CM000680.2:g.23898994A=	GRCh38
NC_000018.9:g.21478958A= , CM000680.1:g.21478958A=	GRCh37
NC_000018.8:g.19732956A=	NCBI36
NG_007853.2:g.214397A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.938A= MANE Plus Clinical	ENSP00000269217.5:p.Asn313=
ENST00000313654.14:c.5765A= MANE Select	ENSP00000324532.8:p.Asn1922=
ENST00000649721.1:c.2657A=	ENSP00000497885.1:p.Asn886=
ENST00000269217.10:c.938A=	ENSP00000269217.5:p.Asn313=
ENST00000313654.13:c.5765A=	ENSP00000324532.8:p.Asn1922=
ENST00000399516.7:c.5765A=	ENSP00000382432.2:p.Asn1922=
ENST00000586709.1:n.153A=
ENST00000586751.5:c.543A=
ENST00000587184.5:c.938A=	ENSP00000466557.1:p.Asn313=
ENST00000588770.5:n.343A=
NM_000227.4:c.938A=	NP_000218.3:p.Asn313=
NM_001127717.2:c.5765A=	NP_001121189.2:p.Asn1922=
NM_001127718.2:c.938A=	NP_001121190.2:p.Asn313=
NM_198129.2:c.5765A=	NP_937762.2:p.Asn1922=
XM_011525978.1:c.5792A=	XP_011524280.1:p.Asn1931=
XM_011525979.1:c.5783A=	XP_011524281.1:p.Asn1928=
XM_011525980.1:c.5774A=	XP_011524282.1:p.Asn1925=
XM_011525981.1:c.5660A=	XP_011524283.1:p.Asn1887=
XM_011525982.1:c.5792A=	XP_011524284.1:p.Asn1931=
XM_011525978.2:c.5792A=	XP_011524280.1:p.Asn1931=
XM_011525979.2:c.5783A=	XP_011524281.1:p.Asn1928=
XM_011525980.2:c.5774A=	XP_011524282.1:p.Asn1925=
XM_011525981.2:c.5660A=	XP_011524283.1:p.Asn1887=
XM_011525982.2:c.5792A=	XP_011524284.1:p.Asn1931=
XM_017025743.1:c.3644A=	XP_016881232.1:p.Asn1215=
XM_017025744.1:c.1334A=	XP_016881233.1:p.Asn445=
XR_001753199.1:n.6033A=
NM_000227.5:c.938A=	NP_000218.3:p.Asn313=
NM_001127717.3:c.5765A=	NP_001121189.2:p.Asn1922=
NM_001127718.3:c.938A=	NP_001121190.2:p.Asn313=
NM_198129.3:c.5765A=	NP_937762.2:p.Asn1922=
NM_000227.6:c.938A= MANE Plus Clinical	NP_000218.3:p.Asn313=
NM_001127717.4:c.5765A=	NP_001121189.2:p.Asn1922=
NM_001127718.4:c.938A=	NP_001121190.2:p.Asn313=
NM_198129.4:c.5765A= MANE Select	NP_937762.2:p.Asn1922=