Canonical Allele Identifier: CA2290334629

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928217A= , CM000680.2:g.23928217A=	GRCh38
NC_000018.9:g.21508181A= , CM000680.1:g.21508181A=	GRCh37
NC_000018.8:g.19762179A=	NCBI36
NG_007853.2:g.243620A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3445A= MANE Plus Clinical	ENSP00000269217.5:p.Lys1149=
ENST00000313654.14:c.8272A= MANE Select	ENSP00000324532.8:p.Lys2758=
ENST00000649721.1:c.4867A=	ENSP00000497885.1:p.Lys1623=
ENST00000269217.10:c.3445A=	ENSP00000269217.5:p.Lys1149=
ENST00000313654.13:c.8272A=	ENSP00000324532.8:p.Lys2758=
ENST00000399516.7:c.8104A=	ENSP00000382432.2:p.Lys2702=
ENST00000586751.5:c.3050A=
ENST00000587184.5:c.3277A=	ENSP00000466557.1:p.Lys1093=
ENST00000588770.5:n.2850A=
NM_000227.4:c.3445A=	NP_000218.3:p.Lys1149=
NM_001127717.2:c.8104A=	NP_001121189.2:p.Lys2702=
NM_001127718.2:c.3277A=	NP_001121190.2:p.Lys1093=
NM_198129.2:c.8272A=	NP_937762.2:p.Lys2758=
XM_011525978.1:c.8299A=	XP_011524280.1:p.Lys2767=
XM_011525979.1:c.8290A=	XP_011524281.1:p.Lys2764=
XM_011525980.1:c.8281A=	XP_011524282.1:p.Lys2761=
XM_011525981.1:c.8167A=	XP_011524283.1:p.Lys2723=
XM_011525982.1:c.8002A=	XP_011524284.1:p.Lys2668=
XM_011525978.2:c.8299A=	XP_011524280.1:p.Lys2767=
XM_011525979.2:c.8290A=	XP_011524281.1:p.Lys2764=
XM_011525980.2:c.8281A=	XP_011524282.1:p.Lys2761=
XM_011525981.2:c.8167A=	XP_011524283.1:p.Lys2723=
XM_011525982.2:c.8002A=	XP_011524284.1:p.Lys2668=
XM_017025743.1:c.6151A=	XP_016881232.1:p.Lys2051=
XM_017025744.1:c.3841A=	XP_016881233.1:p.Lys1281=
XR_001753199.1:n.8540A=
NM_000227.5:c.3445A=	NP_000218.3:p.Lys1149=
NM_001127717.3:c.8104A=	NP_001121189.2:p.Lys2702=
NM_001127718.3:c.3277A=	NP_001121190.2:p.Lys1093=
NM_198129.3:c.8272A=	NP_937762.2:p.Lys2758=
NM_000227.6:c.3445A= MANE Plus Clinical	NP_000218.3:p.Lys1149=
NM_001127717.4:c.8104A=	NP_001121189.2:p.Lys2702=
NM_001127718.4:c.3277A=	NP_001121190.2:p.Lys1093=
NM_198129.4:c.8272A= MANE Select	NP_937762.2:p.Lys2758=