Canonical Allele Identifier: CA2290334612

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928166T= , CM000680.2:g.23928166T=	GRCh38
NC_000018.9:g.21508130T= , CM000680.1:g.21508130T=	GRCh37
NC_000018.8:g.19762128T=	NCBI36
NG_007853.2:g.243569T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3394T= MANE Plus Clinical	ENSP00000269217.5:p.Leu1132=
ENST00000313654.14:c.8221T= MANE Select	ENSP00000324532.8:p.Leu2741=
ENST00000649721.1:c.4816T=	ENSP00000497885.1:p.Leu1606=
ENST00000269217.10:c.3394T=	ENSP00000269217.5:p.Leu1132=
ENST00000313654.13:c.8221T=	ENSP00000324532.8:p.Leu2741=
ENST00000399516.7:c.8053T=	ENSP00000382432.2:p.Leu2685=
ENST00000586751.5:c.2999T=
ENST00000587184.5:c.3226T=	ENSP00000466557.1:p.Leu1076=
ENST00000588770.5:n.2799T=
NM_000227.4:c.3394T=	NP_000218.3:p.Leu1132=
NM_001127717.2:c.8053T=	NP_001121189.2:p.Leu2685=
NM_001127718.2:c.3226T=	NP_001121190.2:p.Leu1076=
NM_198129.2:c.8221T=	NP_937762.2:p.Leu2741=
XM_011525978.1:c.8248T=	XP_011524280.1:p.Leu2750=
XM_011525979.1:c.8239T=	XP_011524281.1:p.Leu2747=
XM_011525980.1:c.8230T=	XP_011524282.1:p.Leu2744=
XM_011525981.1:c.8116T=	XP_011524283.1:p.Leu2706=
XM_011525982.1:c.7951T=	XP_011524284.1:p.Leu2651=
XM_011525978.2:c.8248T=	XP_011524280.1:p.Leu2750=
XM_011525979.2:c.8239T=	XP_011524281.1:p.Leu2747=
XM_011525980.2:c.8230T=	XP_011524282.1:p.Leu2744=
XM_011525981.2:c.8116T=	XP_011524283.1:p.Leu2706=
XM_011525982.2:c.7951T=	XP_011524284.1:p.Leu2651=
XM_017025743.1:c.6100T=	XP_016881232.1:p.Leu2034=
XM_017025744.1:c.3790T=	XP_016881233.1:p.Leu1264=
XR_001753199.1:n.8489T=
NM_000227.5:c.3394T=	NP_000218.3:p.Leu1132=
NM_001127717.3:c.8053T=	NP_001121189.2:p.Leu2685=
NM_001127718.3:c.3226T=	NP_001121190.2:p.Leu1076=
NM_198129.3:c.8221T=	NP_937762.2:p.Leu2741=
NM_000227.6:c.3394T= MANE Plus Clinical	NP_000218.3:p.Leu1132=
NM_001127717.4:c.8053T=	NP_001121189.2:p.Leu2685=
NM_001127718.4:c.3226T=	NP_001121190.2:p.Leu1076=
NM_198129.4:c.8221T= MANE Select	NP_937762.2:p.Leu2741=