Canonical Allele Identifier: CA2290334619

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928187G= , CM000680.2:g.23928187G=	GRCh38
NC_000018.9:g.21508151G= , CM000680.1:g.21508151G=	GRCh37
NC_000018.8:g.19762149G=	NCBI36
NG_007853.2:g.243590G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3415G= MANE Plus Clinical	ENSP00000269217.5:p.Val1139=
ENST00000313654.14:c.8242G= MANE Select	ENSP00000324532.8:p.Val2748=
ENST00000649721.1:c.4837G=	ENSP00000497885.1:p.Val1613=
ENST00000269217.10:c.3415G=	ENSP00000269217.5:p.Val1139=
ENST00000313654.13:c.8242G=	ENSP00000324532.8:p.Val2748=
ENST00000399516.7:c.8074G=	ENSP00000382432.2:p.Val2692=
ENST00000586751.5:c.3020G=
ENST00000587184.5:c.3247G=	ENSP00000466557.1:p.Val1083=
ENST00000588770.5:n.2820G=
NM_000227.4:c.3415G=	NP_000218.3:p.Val1139=
NM_001127717.2:c.8074G=	NP_001121189.2:p.Val2692=
NM_001127718.2:c.3247G=	NP_001121190.2:p.Val1083=
NM_198129.2:c.8242G=	NP_937762.2:p.Val2748=
XM_011525978.1:c.8269G=	XP_011524280.1:p.Val2757=
XM_011525979.1:c.8260G=	XP_011524281.1:p.Val2754=
XM_011525980.1:c.8251G=	XP_011524282.1:p.Val2751=
XM_011525981.1:c.8137G=	XP_011524283.1:p.Val2713=
XM_011525982.1:c.7972G=	XP_011524284.1:p.Val2658=
XM_011525978.2:c.8269G=	XP_011524280.1:p.Val2757=
XM_011525979.2:c.8260G=	XP_011524281.1:p.Val2754=
XM_011525980.2:c.8251G=	XP_011524282.1:p.Val2751=
XM_011525981.2:c.8137G=	XP_011524283.1:p.Val2713=
XM_011525982.2:c.7972G=	XP_011524284.1:p.Val2658=
XM_017025743.1:c.6121G=	XP_016881232.1:p.Val2041=
XM_017025744.1:c.3811G=	XP_016881233.1:p.Val1271=
XR_001753199.1:n.8510G=
NM_000227.5:c.3415G=	NP_000218.3:p.Val1139=
NM_001127717.3:c.8074G=	NP_001121189.2:p.Val2692=
NM_001127718.3:c.3247G=	NP_001121190.2:p.Val1083=
NM_198129.3:c.8242G=	NP_937762.2:p.Val2748=
NM_000227.6:c.3415G= MANE Plus Clinical	NP_000218.3:p.Val1139=
NM_001127717.4:c.8074G=	NP_001121189.2:p.Val2692=
NM_001127718.4:c.3247G=	NP_001121190.2:p.Val1083=
NM_198129.4:c.8242G= MANE Select	NP_937762.2:p.Val2748=