Canonical Allele Identifier: CA2290344150

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950106C= , CM000680.2:g.23950106C=	GRCh38
NC_000018.9:g.21530070C= , CM000680.1:g.21530070C=	GRCh37
NC_000018.8:g.19784068C=	NCBI36
NG_007853.2:g.265509C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4762C= MANE Plus Clinical	ENSP00000269217.5:p.His1588=
ENST00000313654.14:c.9589C= MANE Select	ENSP00000324532.8:p.His3197=
ENST00000649721.1:c.6184C=	ENSP00000497885.1:p.His2062=
ENST00000269217.10:c.4762C=	ENSP00000269217.5:p.His1588=
ENST00000313654.13:c.9589C=	ENSP00000324532.8:p.His3197=
ENST00000399516.7:c.9421C=	ENSP00000382432.2:p.His3141=
ENST00000587184.5:c.4594C=	ENSP00000466557.1:p.His1532=
ENST00000588004.1:c.110C=
ENST00000588770.5:n.4167C=
NM_000227.4:c.4762C=	NP_000218.3:p.His1588=
NM_001127717.2:c.9421C=	NP_001121189.2:p.His3141=
NM_001127718.2:c.4594C=	NP_001121190.2:p.His1532=
NM_198129.2:c.9589C=	NP_937762.2:p.His3197=
XM_011525978.1:c.9616C=	XP_011524280.1:p.His3206=
XM_011525979.1:c.9607C=	XP_011524281.1:p.His3203=
XM_011525980.1:c.9598C=	XP_011524282.1:p.His3200=
XM_011525981.1:c.9484C=	XP_011524283.1:p.His3162=
XM_011525982.1:c.9319C=	XP_011524284.1:p.His3107=
XM_011525978.2:c.9616C=	XP_011524280.1:p.His3206=
XM_011525979.2:c.9607C=	XP_011524281.1:p.His3203=
XM_011525980.2:c.9598C=	XP_011524282.1:p.His3200=
XM_011525981.2:c.9484C=	XP_011524283.1:p.His3162=
XM_011525982.2:c.9319C=	XP_011524284.1:p.His3107=
XM_017025743.1:c.7468C=	XP_016881232.1:p.His2490=
XM_017025744.1:c.5158C=	XP_016881233.1:p.His1720=
XR_001753199.1:n.9857C=
NM_000227.5:c.4762C=	NP_000218.3:p.His1588=
NM_001127717.3:c.9421C=	NP_001121189.2:p.His3141=
NM_001127718.3:c.4594C=	NP_001121190.2:p.His1532=
NM_198129.3:c.9589C=	NP_937762.2:p.His3197=
NM_000227.6:c.4762C= MANE Plus Clinical	NP_000218.3:p.His1588=
NM_001127717.4:c.9421C=	NP_001121189.2:p.His3141=
NM_001127718.4:c.4594C=	NP_001121190.2:p.His1532=
NM_198129.4:c.9589C= MANE Select	NP_937762.2:p.His3197=