Canonical Allele Identifier: CA2290328961

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915365T= , CM000680.2:g.23915365T=	GRCh38
NC_000018.9:g.21495329T= , CM000680.1:g.21495329T=	GRCh37
NC_000018.8:g.19749327T=	NCBI36
NG_007853.2:g.230768T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2894T= MANE Plus Clinical	ENSP00000269217.5:p.Leu965=
ENST00000313654.14:c.7721T= MANE Select	ENSP00000324532.8:p.Leu2574=
ENST00000649721.1:c.4316T=	ENSP00000497885.1:p.Leu1439=
ENST00000269217.10:c.2894T=	ENSP00000269217.5:p.Leu965=
ENST00000313654.13:c.7721T=	ENSP00000324532.8:p.Leu2574=
ENST00000399516.7:c.7553T=	ENSP00000382432.2:p.Leu2518=
ENST00000586751.5:c.2499T=
ENST00000587184.5:c.2726T=	ENSP00000466557.1:p.Leu909=
ENST00000588770.5:n.2299T=
NM_000227.4:c.2894T=	NP_000218.3:p.Leu965=
NM_001127717.2:c.7553T=	NP_001121189.2:p.Leu2518=
NM_001127718.2:c.2726T=	NP_001121190.2:p.Leu909=
NM_198129.2:c.7721T=	NP_937762.2:p.Leu2574=
XM_011525978.1:c.7748T=	XP_011524280.1:p.Leu2583=
XM_011525979.1:c.7739T=	XP_011524281.1:p.Leu2580=
XM_011525980.1:c.7730T=	XP_011524282.1:p.Leu2577=
XM_011525981.1:c.7616T=	XP_011524283.1:p.Leu2539=
XM_011525982.1:c.7451T=	XP_011524284.1:p.Leu2484=
XM_011525978.2:c.7748T=	XP_011524280.1:p.Leu2583=
XM_011525979.2:c.7739T=	XP_011524281.1:p.Leu2580=
XM_011525980.2:c.7730T=	XP_011524282.1:p.Leu2577=
XM_011525981.2:c.7616T=	XP_011524283.1:p.Leu2539=
XM_011525982.2:c.7451T=	XP_011524284.1:p.Leu2484=
XM_017025743.1:c.5600T=	XP_016881232.1:p.Leu1867=
XM_017025744.1:c.3290T=	XP_016881233.1:p.Leu1097=
XR_001753199.1:n.7989T=
NM_000227.5:c.2894T=	NP_000218.3:p.Leu965=
NM_001127717.3:c.7553T=	NP_001121189.2:p.Leu2518=
NM_001127718.3:c.2726T=	NP_001121190.2:p.Leu909=
NM_198129.3:c.7721T=	NP_937762.2:p.Leu2574=
NM_000227.6:c.2894T= MANE Plus Clinical	NP_000218.3:p.Leu965=
NM_001127717.4:c.7553T=	NP_001121189.2:p.Leu2518=
NM_001127718.4:c.2726T=	NP_001121190.2:p.Leu909=
NM_198129.4:c.7721T= MANE Select	NP_937762.2:p.Leu2574=