Canonical Allele Identifier: CA2811822937

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915383_23915384insCCCCCAAAC , CM000680.2:g.23915383_23915384insCCCCCAAAC	GRCh38
NC_000018.9:g.21495347_21495348insCCCCCAAAC , CM000680.1:g.21495347_21495348insCCCCCAAAC	GRCh37
NC_000018.8:g.19749345_19749346insCCCCCAAAC	NCBI36
NG_007853.2:g.230786_230787insCCCCCAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2912_2913insCCCCCAAAC MANE Plus Clinical	ENSP00000269217.5:p.Thr971_Phe972insProGlnThr
ENST00000313654.14:c.7739_7740insCCCCCAAAC MANE Select	ENSP00000324532.8:p.Thr2580_Phe2581insProGlnThr
ENST00000649721.1:c.4334_4335insCCCCCAAAC	ENSP00000497885.1:p.Thr1445_Phe1446insProGlnThr
ENST00000269217.10:c.2912_2913insCCCCCAAAC	ENSP00000269217.5:p.Thr971_Phe972insProGlnThr
ENST00000313654.13:c.7739_7740insCCCCCAAAC	ENSP00000324532.8:p.Thr2580_Phe2581insProGlnThr
ENST00000399516.7:c.7571_7572insCCCCCAAAC	ENSP00000382432.2:p.Thr2524_Phe2525insProGlnThr
ENST00000586751.5:c.2517_2518insCCCCCAAAC
ENST00000587184.5:c.2744_2745insCCCCCAAAC	ENSP00000466557.1:p.Thr915_Phe916insProGlnThr
ENST00000588770.5:n.2317_2318insCCCCCAAAC
NM_000227.4:c.2912_2913insCCCCCAAAC	NP_000218.3:p.Thr971_Phe972insProGlnThr
NM_001127717.2:c.7571_7572insCCCCCAAAC	NP_001121189.2:p.Thr2524_Phe2525insProGlnThr
NM_001127718.2:c.2744_2745insCCCCCAAAC	NP_001121190.2:p.Thr915_Phe916insProGlnThr
NM_198129.2:c.7739_7740insCCCCCAAAC	NP_937762.2:p.Thr2580_Phe2581insProGlnThr
XM_011525978.1:c.7766_7767insCCCCCAAAC	XP_011524280.1:p.Thr2589_Phe2590insProGlnThr
XM_011525979.1:c.7757_7758insCCCCCAAAC	XP_011524281.1:p.Thr2586_Phe2587insProGlnThr
XM_011525980.1:c.7748_7749insCCCCCAAAC	XP_011524282.1:p.Thr2583_Phe2584insProGlnThr
XM_011525981.1:c.7634_7635insCCCCCAAAC	XP_011524283.1:p.Thr2545_Phe2546insProGlnThr
XM_011525982.1:c.7469_7470insCCCCCAAAC	XP_011524284.1:p.Thr2490_Phe2491insProGlnThr
XM_011525978.2:c.7766_7767insCCCCCAAAC	XP_011524280.1:p.Thr2589_Phe2590insProGlnThr
XM_011525979.2:c.7757_7758insCCCCCAAAC	XP_011524281.1:p.Thr2586_Phe2587insProGlnThr
XM_011525980.2:c.7748_7749insCCCCCAAAC	XP_011524282.1:p.Thr2583_Phe2584insProGlnThr
XM_011525981.2:c.7634_7635insCCCCCAAAC	XP_011524283.1:p.Thr2545_Phe2546insProGlnThr
XM_011525982.2:c.7469_7470insCCCCCAAAC	XP_011524284.1:p.Thr2490_Phe2491insProGlnThr
XM_017025743.1:c.5618_5619insCCCCCAAAC	XP_016881232.1:p.Thr1873_Phe1874insProGlnThr
XM_017025744.1:c.3308_3309insCCCCCAAAC	XP_016881233.1:p.Thr1103_Phe1104insProGlnThr
XR_001753199.1:n.8007_8008insCCCCCAAAC
NM_000227.5:c.2912_2913insCCCCCAAAC	NP_000218.3:p.Thr971_Phe972insProGlnThr
NM_001127717.3:c.7571_7572insCCCCCAAAC	NP_001121189.2:p.Thr2524_Phe2525insProGlnThr
NM_001127718.3:c.2744_2745insCCCCCAAAC	NP_001121190.2:p.Thr915_Phe916insProGlnThr
NM_198129.3:c.7739_7740insCCCCCAAAC	NP_937762.2:p.Thr2580_Phe2581insProGlnThr
NM_000227.6:c.2912_2913insCCCCCAAAC MANE Plus Clinical	NP_000218.3:p.Thr971_Phe972insProGlnThr
NM_001127717.4:c.7571_7572insCCCCCAAAC	NP_001121189.2:p.Thr2524_Phe2525insProGlnThr
NM_001127718.4:c.2744_2745insCCCCCAAAC	NP_001121190.2:p.Thr915_Phe916insProGlnThr
NM_198129.4:c.7739_7740insCCCCCAAAC MANE Select	NP_937762.2:p.Thr2580_Phe2581insProGlnThr