Canonical Allele Identifier: CA2290322158

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898739A= , CM000680.2:g.23898739A=	GRCh38
NC_000018.9:g.21478703A= , CM000680.1:g.21478703A=	GRCh37
NC_000018.8:g.19732701A=	NCBI36
NG_007853.2:g.214142A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.788A= MANE Plus Clinical	ENSP00000269217.5:p.Asn263=
ENST00000313654.14:c.5615A= MANE Select	ENSP00000324532.8:p.Asn1872=
ENST00000649721.1:c.2507A=	ENSP00000497885.1:p.Asn836=
ENST00000269217.10:c.788A=	ENSP00000269217.5:p.Asn263=
ENST00000313654.13:c.5615A=	ENSP00000324532.8:p.Asn1872=
ENST00000399516.7:c.5615A=	ENSP00000382432.2:p.Asn1872=
ENST00000586709.1:n.3A=
ENST00000586751.5:c.393A=
ENST00000587184.5:c.788A=	ENSP00000466557.1:p.Asn263=
ENST00000588770.5:n.193A=
NM_000227.4:c.788A=	NP_000218.3:p.Asn263=
NM_001127717.2:c.5615A=	NP_001121189.2:p.Asn1872=
NM_001127718.2:c.788A=	NP_001121190.2:p.Asn263=
NM_198129.2:c.5615A=	NP_937762.2:p.Asn1872=
XM_011525978.1:c.5642A=	XP_011524280.1:p.Asn1881=
XM_011525979.1:c.5633A=	XP_011524281.1:p.Asn1878=
XM_011525980.1:c.5624A=	XP_011524282.1:p.Asn1875=
XM_011525981.1:c.5510A=	XP_011524283.1:p.Asn1837=
XM_011525982.1:c.5642A=	XP_011524284.1:p.Asn1881=
XM_011525978.2:c.5642A=	XP_011524280.1:p.Asn1881=
XM_011525979.2:c.5633A=	XP_011524281.1:p.Asn1878=
XM_011525980.2:c.5624A=	XP_011524282.1:p.Asn1875=
XM_011525981.2:c.5510A=	XP_011524283.1:p.Asn1837=
XM_011525982.2:c.5642A=	XP_011524284.1:p.Asn1881=
XM_017025743.1:c.3494A=	XP_016881232.1:p.Asn1165=
XM_017025744.1:c.1184A=	XP_016881233.1:p.Asn395=
XR_001753199.1:n.5883A=
NM_000227.5:c.788A=	NP_000218.3:p.Asn263=
NM_001127717.3:c.5615A=	NP_001121189.2:p.Asn1872=
NM_001127718.3:c.788A=	NP_001121190.2:p.Asn263=
NM_198129.3:c.5615A=	NP_937762.2:p.Asn1872=
NM_000227.6:c.788A= MANE Plus Clinical	NP_000218.3:p.Asn263=
NM_001127717.4:c.5615A=	NP_001121189.2:p.Asn1872=
NM_001127718.4:c.788A=	NP_001121190.2:p.Asn263=
NM_198129.4:c.5615A= MANE Select	NP_937762.2:p.Asn1872=