Canonical Allele Identifier: CA2290334613

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928173A= , CM000680.2:g.23928173A=	GRCh38
NC_000018.9:g.21508137A= , CM000680.1:g.21508137A=	GRCh37
NC_000018.8:g.19762135A=	NCBI36
NG_007853.2:g.243576A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3401A= MANE Plus Clinical	ENSP00000269217.5:p.Lys1134=
ENST00000313654.14:c.8228A= MANE Select	ENSP00000324532.8:p.Lys2743=
ENST00000649721.1:c.4823A=	ENSP00000497885.1:p.Lys1608=
ENST00000269217.10:c.3401A=	ENSP00000269217.5:p.Lys1134=
ENST00000313654.13:c.8228A=	ENSP00000324532.8:p.Lys2743=
ENST00000399516.7:c.8060A=	ENSP00000382432.2:p.Lys2687=
ENST00000586751.5:c.3006A=
ENST00000587184.5:c.3233A=	ENSP00000466557.1:p.Lys1078=
ENST00000588770.5:n.2806A=
NM_000227.4:c.3401A=	NP_000218.3:p.Lys1134=
NM_001127717.2:c.8060A=	NP_001121189.2:p.Lys2687=
NM_001127718.2:c.3233A=	NP_001121190.2:p.Lys1078=
NM_198129.2:c.8228A=	NP_937762.2:p.Lys2743=
XM_011525978.1:c.8255A=	XP_011524280.1:p.Lys2752=
XM_011525979.1:c.8246A=	XP_011524281.1:p.Lys2749=
XM_011525980.1:c.8237A=	XP_011524282.1:p.Lys2746=
XM_011525981.1:c.8123A=	XP_011524283.1:p.Lys2708=
XM_011525982.1:c.7958A=	XP_011524284.1:p.Lys2653=
XM_011525978.2:c.8255A=	XP_011524280.1:p.Lys2752=
XM_011525979.2:c.8246A=	XP_011524281.1:p.Lys2749=
XM_011525980.2:c.8237A=	XP_011524282.1:p.Lys2746=
XM_011525981.2:c.8123A=	XP_011524283.1:p.Lys2708=
XM_011525982.2:c.7958A=	XP_011524284.1:p.Lys2653=
XM_017025743.1:c.6107A=	XP_016881232.1:p.Lys2036=
XM_017025744.1:c.3797A=	XP_016881233.1:p.Lys1266=
XR_001753199.1:n.8496A=
NM_000227.5:c.3401A=	NP_000218.3:p.Lys1134=
NM_001127717.3:c.8060A=	NP_001121189.2:p.Lys2687=
NM_001127718.3:c.3233A=	NP_001121190.2:p.Lys1078=
NM_198129.3:c.8228A=	NP_937762.2:p.Lys2743=
NM_000227.6:c.3401A= MANE Plus Clinical	NP_000218.3:p.Lys1134=
NM_001127717.4:c.8060A=	NP_001121189.2:p.Lys2687=
NM_001127718.4:c.3233A=	NP_001121190.2:p.Lys1078=
NM_198129.4:c.8228A= MANE Select	NP_937762.2:p.Lys2743=