Canonical Allele Identifier: CA2290328995

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915394A= , CM000680.2:g.23915394A=	GRCh38
NC_000018.9:g.21495358A= , CM000680.1:g.21495358A=	GRCh37
NC_000018.8:g.19749356A=	NCBI36
NG_007853.2:g.230797A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2923A= MANE Plus Clinical	ENSP00000269217.5:p.Asn975=
ENST00000313654.14:c.7750A= MANE Select	ENSP00000324532.8:p.Asn2584=
ENST00000649721.1:c.4345A=	ENSP00000497885.1:p.Asn1449=
ENST00000269217.10:c.2923A=	ENSP00000269217.5:p.Asn975=
ENST00000313654.13:c.7750A=	ENSP00000324532.8:p.Asn2584=
ENST00000399516.7:c.7582A=	ENSP00000382432.2:p.Asn2528=
ENST00000586751.5:c.2528A=
ENST00000587184.5:c.2755A=	ENSP00000466557.1:p.Asn919=
ENST00000588770.5:n.2328A=
NM_000227.4:c.2923A=	NP_000218.3:p.Asn975=
NM_001127717.2:c.7582A=	NP_001121189.2:p.Asn2528=
NM_001127718.2:c.2755A=	NP_001121190.2:p.Asn919=
NM_198129.2:c.7750A=	NP_937762.2:p.Asn2584=
XM_011525978.1:c.7777A=	XP_011524280.1:p.Asn2593=
XM_011525979.1:c.7768A=	XP_011524281.1:p.Asn2590=
XM_011525980.1:c.7759A=	XP_011524282.1:p.Asn2587=
XM_011525981.1:c.7645A=	XP_011524283.1:p.Asn2549=
XM_011525982.1:c.7480A=	XP_011524284.1:p.Asn2494=
XM_011525978.2:c.7777A=	XP_011524280.1:p.Asn2593=
XM_011525979.2:c.7768A=	XP_011524281.1:p.Asn2590=
XM_011525980.2:c.7759A=	XP_011524282.1:p.Asn2587=
XM_011525981.2:c.7645A=	XP_011524283.1:p.Asn2549=
XM_011525982.2:c.7480A=	XP_011524284.1:p.Asn2494=
XM_017025743.1:c.5629A=	XP_016881232.1:p.Asn1877=
XM_017025744.1:c.3319A=	XP_016881233.1:p.Asn1107=
XR_001753199.1:n.8018A=
NM_000227.5:c.2923A=	NP_000218.3:p.Asn975=
NM_001127717.3:c.7582A=	NP_001121189.2:p.Asn2528=
NM_001127718.3:c.2755A=	NP_001121190.2:p.Asn919=
NM_198129.3:c.7750A=	NP_937762.2:p.Asn2584=
NM_000227.6:c.2923A= MANE Plus Clinical	NP_000218.3:p.Asn975=
NM_001127717.4:c.7582A=	NP_001121189.2:p.Asn2528=
NM_001127718.4:c.2755A=	NP_001121190.2:p.Asn919=
NM_198129.4:c.7750A= MANE Select	NP_937762.2:p.Asn2584=