Canonical Allele Identifier: CA2290334628

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928215C= , CM000680.2:g.23928215C=	GRCh38
NC_000018.9:g.21508179C= , CM000680.1:g.21508179C=	GRCh37
NC_000018.8:g.19762177C=	NCBI36
NG_007853.2:g.243618C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3443C= MANE Plus Clinical	ENSP00000269217.5:p.Thr1148=
ENST00000313654.14:c.8270C= MANE Select	ENSP00000324532.8:p.Thr2757=
ENST00000649721.1:c.4865C=	ENSP00000497885.1:p.Thr1622=
ENST00000269217.10:c.3443C=	ENSP00000269217.5:p.Thr1148=
ENST00000313654.13:c.8270C=	ENSP00000324532.8:p.Thr2757=
ENST00000399516.7:c.8102C=	ENSP00000382432.2:p.Thr2701=
ENST00000586751.5:c.3048C=
ENST00000587184.5:c.3275C=	ENSP00000466557.1:p.Thr1092=
ENST00000588770.5:n.2848C=
NM_000227.4:c.3443C=	NP_000218.3:p.Thr1148=
NM_001127717.2:c.8102C=	NP_001121189.2:p.Thr2701=
NM_001127718.2:c.3275C=	NP_001121190.2:p.Thr1092=
NM_198129.2:c.8270C=	NP_937762.2:p.Thr2757=
XM_011525978.1:c.8297C=	XP_011524280.1:p.Thr2766=
XM_011525979.1:c.8288C=	XP_011524281.1:p.Thr2763=
XM_011525980.1:c.8279C=	XP_011524282.1:p.Thr2760=
XM_011525981.1:c.8165C=	XP_011524283.1:p.Thr2722=
XM_011525982.1:c.8000C=	XP_011524284.1:p.Thr2667=
XM_011525978.2:c.8297C=	XP_011524280.1:p.Thr2766=
XM_011525979.2:c.8288C=	XP_011524281.1:p.Thr2763=
XM_011525980.2:c.8279C=	XP_011524282.1:p.Thr2760=
XM_011525981.2:c.8165C=	XP_011524283.1:p.Thr2722=
XM_011525982.2:c.8000C=	XP_011524284.1:p.Thr2667=
XM_017025743.1:c.6149C=	XP_016881232.1:p.Thr2050=
XM_017025744.1:c.3839C=	XP_016881233.1:p.Thr1280=
XR_001753199.1:n.8538C=
NM_000227.5:c.3443C=	NP_000218.3:p.Thr1148=
NM_001127717.3:c.8102C=	NP_001121189.2:p.Thr2701=
NM_001127718.3:c.3275C=	NP_001121190.2:p.Thr1092=
NM_198129.3:c.8270C=	NP_937762.2:p.Thr2757=
NM_000227.6:c.3443C= MANE Plus Clinical	NP_000218.3:p.Thr1148=
NM_001127717.4:c.8102C=	NP_001121189.2:p.Thr2701=
NM_001127718.4:c.3275C=	NP_001121190.2:p.Thr1092=
NM_198129.4:c.8270C= MANE Select	NP_937762.2:p.Thr2757=