Canonical Allele Identifier: CA2290323928

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903037A= , CM000680.2:g.23903037A=	GRCh38
NC_000018.9:g.21483001A= , CM000680.1:g.21483001A=	GRCh37
NC_000018.8:g.19736999A=	NCBI36
NG_007853.2:g.218440A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1403A= MANE Plus Clinical	ENSP00000269217.5:p.Gln468=
ENST00000313654.14:c.6230A= MANE Select	ENSP00000324532.8:p.Gln2077=
ENST00000649721.1:c.3122A=	ENSP00000497885.1:p.Gln1041=
ENST00000269217.10:c.1403A=	ENSP00000269217.5:p.Gln468=
ENST00000313654.13:c.6230A=	ENSP00000324532.8:p.Gln2077=
ENST00000399516.7:c.6062A=	ENSP00000382432.2:p.Gln2021=
ENST00000586751.5:c.1008A=
ENST00000587184.5:c.1235A=	ENSP00000466557.1:p.Gln412=
ENST00000588770.5:n.808A=
NM_000227.4:c.1403A=	NP_000218.3:p.Gln468=
NM_001127717.2:c.6062A=	NP_001121189.2:p.Gln2021=
NM_001127718.2:c.1235A=	NP_001121190.2:p.Gln412=
NM_198129.2:c.6230A=	NP_937762.2:p.Gln2077=
XM_011525978.1:c.6257A=	XP_011524280.1:p.Gln2086=
XM_011525979.1:c.6248A=	XP_011524281.1:p.Gln2083=
XM_011525980.1:c.6239A=	XP_011524282.1:p.Gln2080=
XM_011525981.1:c.6125A=	XP_011524283.1:p.Gln2042=
XM_011525982.1:c.6257A=	XP_011524284.1:p.Gln2086=
XM_011525978.2:c.6257A=	XP_011524280.1:p.Gln2086=
XM_011525979.2:c.6248A=	XP_011524281.1:p.Gln2083=
XM_011525980.2:c.6239A=	XP_011524282.1:p.Gln2080=
XM_011525981.2:c.6125A=	XP_011524283.1:p.Gln2042=
XM_011525982.2:c.6257A=	XP_011524284.1:p.Gln2086=
XM_017025743.1:c.4109A=	XP_016881232.1:p.Gln1370=
XM_017025744.1:c.1799A=	XP_016881233.1:p.Gln600=
XR_001753199.1:n.6498A=
NM_000227.5:c.1403A=	NP_000218.3:p.Gln468=
NM_001127717.3:c.6062A=	NP_001121189.2:p.Gln2021=
NM_001127718.3:c.1235A=	NP_001121190.2:p.Gln412=
NM_198129.3:c.6230A=	NP_937762.2:p.Gln2077=
NM_000227.6:c.1403A= MANE Plus Clinical	NP_000218.3:p.Gln468=
NM_001127717.4:c.6062A=	NP_001121189.2:p.Gln2021=
NM_001127718.4:c.1235A=	NP_001121190.2:p.Gln412=
NM_198129.4:c.6230A= MANE Select	NP_937762.2:p.Gln2077=