Canonical Allele Identifier: CA2290344088

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23950074T= , CM000680.2:g.23950074T=	GRCh38
NC_000018.9:g.21530038T= , CM000680.1:g.21530038T=	GRCh37
NC_000018.8:g.19784036T=	NCBI36
NG_007853.2:g.265477T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4730T= MANE Plus Clinical	ENSP00000269217.5:p.Ile1577=
ENST00000313654.14:c.9557T= MANE Select	ENSP00000324532.8:p.Ile3186=
ENST00000649721.1:c.6152T=	ENSP00000497885.1:p.Ile2051=
ENST00000269217.10:c.4730T=	ENSP00000269217.5:p.Ile1577=
ENST00000313654.13:c.9557T=	ENSP00000324532.8:p.Ile3186=
ENST00000399516.7:c.9389T=	ENSP00000382432.2:p.Ile3130=
ENST00000587184.5:c.4562T=	ENSP00000466557.1:p.Ile1521=
ENST00000588004.1:c.78T=
ENST00000588770.5:n.4135T=
NM_000227.4:c.4730T=	NP_000218.3:p.Ile1577=
NM_001127717.2:c.9389T=	NP_001121189.2:p.Ile3130=
NM_001127718.2:c.4562T=	NP_001121190.2:p.Ile1521=
NM_198129.2:c.9557T=	NP_937762.2:p.Ile3186=
XM_011525978.1:c.9584T=	XP_011524280.1:p.Ile3195=
XM_011525979.1:c.9575T=	XP_011524281.1:p.Ile3192=
XM_011525980.1:c.9566T=	XP_011524282.1:p.Ile3189=
XM_011525981.1:c.9452T=	XP_011524283.1:p.Ile3151=
XM_011525982.1:c.9287T=	XP_011524284.1:p.Ile3096=
XM_011525978.2:c.9584T=	XP_011524280.1:p.Ile3195=
XM_011525979.2:c.9575T=	XP_011524281.1:p.Ile3192=
XM_011525980.2:c.9566T=	XP_011524282.1:p.Ile3189=
XM_011525981.2:c.9452T=	XP_011524283.1:p.Ile3151=
XM_011525982.2:c.9287T=	XP_011524284.1:p.Ile3096=
XM_017025743.1:c.7436T=	XP_016881232.1:p.Ile2479=
XM_017025744.1:c.5126T=	XP_016881233.1:p.Ile1709=
XR_001753199.1:n.9825T=
NM_000227.5:c.4730T=	NP_000218.3:p.Ile1577=
NM_001127717.3:c.9389T=	NP_001121189.2:p.Ile3130=
NM_001127718.3:c.4562T=	NP_001121190.2:p.Ile1521=
NM_198129.3:c.9557T=	NP_937762.2:p.Ile3186=
NM_000227.6:c.4730T= MANE Plus Clinical	NP_000218.3:p.Ile1577=
NM_001127717.4:c.9389T=	NP_001121189.2:p.Ile3130=
NM_001127718.4:c.4562T=	NP_001121190.2:p.Ile1521=
NM_198129.4:c.9557T= MANE Select	NP_937762.2:p.Ile3186=