Canonical Allele Identifier: CA2290334635

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928228G= , CM000680.2:g.23928228G=	GRCh38
NC_000018.9:g.21508192G= , CM000680.1:g.21508192G=	GRCh37
NC_000018.8:g.19762190G=	NCBI36
NG_007853.2:g.243631G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3456G= MANE Plus Clinical	ENSP00000269217.5:p.Ser1152=
ENST00000313654.14:c.8283G= MANE Select	ENSP00000324532.8:p.Ser2761=
ENST00000649721.1:c.4878G=	ENSP00000497885.1:p.Ser1626=
ENST00000269217.10:c.3456G=	ENSP00000269217.5:p.Ser1152=
ENST00000313654.13:c.8283G=	ENSP00000324532.8:p.Ser2761=
ENST00000399516.7:c.8115G=	ENSP00000382432.2:p.Ser2705=
ENST00000586751.5:c.3061G=
ENST00000587184.5:c.3288G=	ENSP00000466557.1:p.Ser1096=
ENST00000588770.5:n.2861G=
NM_000227.4:c.3456G=	NP_000218.3:p.Ser1152=
NM_001127717.2:c.8115G=	NP_001121189.2:p.Ser2705=
NM_001127718.2:c.3288G=	NP_001121190.2:p.Ser1096=
NM_198129.2:c.8283G=	NP_937762.2:p.Ser2761=
XM_011525978.1:c.8310G=	XP_011524280.1:p.Ser2770=
XM_011525979.1:c.8301G=	XP_011524281.1:p.Ser2767=
XM_011525980.1:c.8292G=	XP_011524282.1:p.Ser2764=
XM_011525981.1:c.8178G=	XP_011524283.1:p.Ser2726=
XM_011525982.1:c.8013G=	XP_011524284.1:p.Ser2671=
XM_011525978.2:c.8310G=	XP_011524280.1:p.Ser2770=
XM_011525979.2:c.8301G=	XP_011524281.1:p.Ser2767=
XM_011525980.2:c.8292G=	XP_011524282.1:p.Ser2764=
XM_011525981.2:c.8178G=	XP_011524283.1:p.Ser2726=
XM_011525982.2:c.8013G=	XP_011524284.1:p.Ser2671=
XM_017025743.1:c.6162G=	XP_016881232.1:p.Ser2054=
XM_017025744.1:c.3852G=	XP_016881233.1:p.Ser1284=
XR_001753199.1:n.8551G=
NM_000227.5:c.3456G=	NP_000218.3:p.Ser1152=
NM_001127717.3:c.8115G=	NP_001121189.2:p.Ser2705=
NM_001127718.3:c.3288G=	NP_001121190.2:p.Ser1096=
NM_198129.3:c.8283G=	NP_937762.2:p.Ser2761=
NM_000227.6:c.3456G= MANE Plus Clinical	NP_000218.3:p.Ser1152=
NM_001127717.4:c.8115G=	NP_001121189.2:p.Ser2705=
NM_001127718.4:c.3288G=	NP_001121190.2:p.Ser1096=
NM_198129.4:c.8283G= MANE Select	NP_937762.2:p.Ser2761=