Canonical Allele Identifier: CA2553116447

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23931064_23931065insGAGTCTTGCTCTCTTGC , CM000680.2:g.23931064_23931065insGAGTCTTGCTCTCTTGC	GRCh38
NC_000018.9:g.21511028_21511029insGAGTCTTGCTCTCTTGC , CM000680.1:g.21511028_21511029insGAGTCTTGCTCTCTTGC	GRCh37
NC_000018.8:g.19765026_19765027insGAGTCTTGCTCTCTTGC	NCBI36
NG_007853.2:g.246467_246468insGAGTCTTGCTCTCTTGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3612_3613insGAGTCTTGCTCTCTTGC MANE Plus Clinical	ENSP00000269217.5:p.Arg1205GlufsTer20
ENST00000313654.14:c.8439_8440insGAGTCTTGCTCTCTTGC MANE Select	ENSP00000324532.8:p.Arg2814GlufsTer20
ENST00000649721.1:c.5034_5035insGAGTCTTGCTCTCTTGC	ENSP00000497885.1:p.Arg1679GlufsTer20
ENST00000269217.10:c.3612_3613insGAGTCTTGCTCTCTTGC	ENSP00000269217.5:p.Arg1205GlufsTer20
ENST00000313654.13:c.8439_8440insGAGTCTTGCTCTCTTGC	ENSP00000324532.8:p.Arg2814GlufsTer20
ENST00000399516.7:c.8271_8272insGAGTCTTGCTCTCTTGC	ENSP00000382432.2:p.Arg2758GlufsTer20
ENST00000586751.5:c.3217_3218insGAGTCTTGCTCTCTTGC
ENST00000587184.5:c.3444_3445insGAGTCTTGCTCTCTTGC	ENSP00000466557.1:p.Arg1149GlufsTer20
ENST00000588164.2:c.144_145insGAGTCTTGCTCTCTTGC	ENSP00000467473.2:p.Arg49GlufsTer20
ENST00000588770.5:n.3017_3018insGAGTCTTGCTCTCTTGC
NM_000227.4:c.3612_3613insGAGTCTTGCTCTCTTGC	NP_000218.3:p.Arg1205GlufsTer20
NM_001127717.2:c.8271_8272insGAGTCTTGCTCTCTTGC	NP_001121189.2:p.Arg2758GlufsTer20
NM_001127718.2:c.3444_3445insGAGTCTTGCTCTCTTGC	NP_001121190.2:p.Arg1149GlufsTer20
NM_198129.2:c.8439_8440insGAGTCTTGCTCTCTTGC	NP_937762.2:p.Arg2814GlufsTer20
XM_011525978.1:c.8466_8467insGAGTCTTGCTCTCTTGC	XP_011524280.1:p.Arg2823GlufsTer20
XM_011525979.1:c.8457_8458insGAGTCTTGCTCTCTTGC	XP_011524281.1:p.Arg2820GlufsTer20
XM_011525980.1:c.8448_8449insGAGTCTTGCTCTCTTGC	XP_011524282.1:p.Arg2817GlufsTer20
XM_011525981.1:c.8334_8335insGAGTCTTGCTCTCTTGC	XP_011524283.1:p.Arg2779GlufsTer20
XM_011525982.1:c.8169_8170insGAGTCTTGCTCTCTTGC	XP_011524284.1:p.Arg2724GlufsTer20
XM_011525978.2:c.8466_8467insGAGTCTTGCTCTCTTGC	XP_011524280.1:p.Arg2823GlufsTer20
XM_011525979.2:c.8457_8458insGAGTCTTGCTCTCTTGC	XP_011524281.1:p.Arg2820GlufsTer20
XM_011525980.2:c.8448_8449insGAGTCTTGCTCTCTTGC	XP_011524282.1:p.Arg2817GlufsTer20
XM_011525981.2:c.8334_8335insGAGTCTTGCTCTCTTGC	XP_011524283.1:p.Arg2779GlufsTer20
XM_011525982.2:c.8169_8170insGAGTCTTGCTCTCTTGC	XP_011524284.1:p.Arg2724GlufsTer20
XM_017025743.1:c.6318_6319insGAGTCTTGCTCTCTTGC	XP_016881232.1:p.Arg2107GlufsTer20
XM_017025744.1:c.4008_4009insGAGTCTTGCTCTCTTGC	XP_016881233.1:p.Arg1337GlufsTer20
XR_001753199.1:n.8707_8708insGAGTCTTGCTCTCTTGC
NM_000227.5:c.3612_3613insGAGTCTTGCTCTCTTGC	NP_000218.3:p.Arg1205GlufsTer20
NM_001127717.3:c.8271_8272insGAGTCTTGCTCTCTTGC	NP_001121189.2:p.Arg2758GlufsTer20
NM_001127718.3:c.3444_3445insGAGTCTTGCTCTCTTGC	NP_001121190.2:p.Arg1149GlufsTer20
NM_198129.3:c.8439_8440insGAGTCTTGCTCTCTTGC	NP_937762.2:p.Arg2814GlufsTer20
NM_000227.6:c.3612_3613insGAGTCTTGCTCTCTTGC MANE Plus Clinical	NP_000218.3:p.Arg1205GlufsTer20
NM_001127717.4:c.8271_8272insGAGTCTTGCTCTCTTGC	NP_001121189.2:p.Arg2758GlufsTer20
NM_001127718.4:c.3444_3445insGAGTCTTGCTCTCTTGC	NP_001121190.2:p.Arg1149GlufsTer20
NM_198129.4:c.8439_8440insGAGTCTTGCTCTCTTGC MANE Select	NP_937762.2:p.Arg2814GlufsTer20