Canonical Allele Identifier: CA2579304147

Gene: FREM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.14784589_14784591dup , CM000671.2:g.14784589_14784591dup	GRCh38
NC_000009.11:g.14784587_14784589dup , CM000671.1:g.14784587_14784589dup	GRCh37
NC_000009.10:g.14774587_14774589dup	NCBI36
NG_017005.2:g.130647_130649dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380880.4:c.4222_4224dup MANE Select	ENSP00000370262.3:p.Asp1408_Arg1409insAsp
ENST00000380875.7:c.3981+8153_3981+8155dup	ENSP00000370257.3:n.3981+8153_3981+8155dup
ENST00000380880.3:c.4222_4224dup	ENSP00000370262.3:p.Asp1408_Arg1409insAsp
ENST00000422223.6:c.4222_4224dup	ENSP00000412940.2:p.Asp1408_Arg1409insAsp
ENST00000466679.1:n.252_254dup
ENST00000485068.5:n.45_47dup
ENST00000497634.2:n.383_385dup
NM_144966.5:c.4222_4224dup	NP_659403.4:p.Asp1408_Arg1409insAsp
XM_005251382.2:c.4222_4224dup	XP_005251439.1:p.Asp1408_Arg1409insAsp
XM_006716726.2:c.4222_4224dup	XP_006716789.1:p.Asp1408_Arg1409insAsp
XM_011517748.1:c.4222_4224dup	XP_011516050.1:p.Asp1408_Arg1409insAsp
XM_011517749.1:c.4222_4224dup	XP_011516051.1:p.Asp1408_Arg1409insAsp
XM_011517750.1:c.4222_4224dup	XP_011516052.1:p.Asp1408_Arg1409insAsp
XM_011517751.1:c.4222_4224dup	XP_011516053.1:p.Asp1408_Arg1409insAsp
XM_011517752.1:c.4222_4224dup	XP_011516054.1:p.Asp1408_Arg1409insAsp
XM_011517753.1:c.4222_4224dup	XP_011516055.1:p.Asp1408_Arg1409insAsp
XM_011517754.1:c.4222_4224dup	XP_011516056.1:p.Asp1408_Arg1409insAsp
XM_011517755.1:c.4222_4224dup	XP_011516057.1:p.Asp1408_Arg1409insAsp
XM_011517756.1:c.4222_4224dup	XP_011516058.1:p.Asp1408_Arg1409insAsp
XR_929188.1:n.5008_5010dup
XR_929190.1:n.5111_5113dup
XR_929487.1:n.89+4572_89+4574dup
XM_005251382.4:c.4222_4224dup	XP_005251439.1:p.Asp1408_Arg1409insAsp
XM_005251384.4:c.-224_-222dup	XP_005251441.1:n.-224_-222dup
XM_006716729.3:c.-221_-219dup	XP_006716792.1:n.-221_-219dup
XM_017014316.2:c.4249_4251dup	XP_016869805.1:p.Asp1417_Arg1418insAsp
XM_017014317.1:c.4249_4251dup	XP_016869806.1:p.Asp1417_Arg1418insAsp
XM_017014319.2:c.4249_4251dup	XP_016869808.1:p.Asp1417_Arg1418insAsp
XM_017014320.2:c.4249_4251dup	XP_016869809.1:p.Asp1417_Arg1418insAsp
XM_017014321.2:c.4249_4251dup	XP_016869810.1:p.Asp1417_Arg1418insAsp
XM_017014322.1:c.4249_4251dup	XP_016869811.1:p.Asp1417_Arg1418insAsp
XM_017014323.1:c.4249_4251dup	XP_016869812.1:p.Asp1417_Arg1418insAsp
XM_017014324.2:c.4249_4251dup	XP_016869813.1:p.Asp1417_Arg1418insAsp
XM_017014325.2:c.4249_4251dup	XP_016869814.1:p.Asp1417_Arg1418insAsp
XM_017014326.1:c.3841_3843dup	XP_016869815.1:p.Asp1281_Arg1282insAsp
XM_017014327.2:c.3325_3327dup	XP_016869816.1:p.Asp1109_Arg1110insAsp
XM_017014328.2:c.4249_4251dup	XP_016869817.1:p.Asp1417_Arg1418insAsp
XM_017014329.2:c.4249_4251dup	XP_016869818.1:p.Asp1417_Arg1418insAsp
XR_001746194.2:n.5035_5037dup
XR_001746195.2:n.5035_5037dup
XR_001746196.2:n.5138_5140dup
XR_001746197.2:n.5031_5033dup
NR_163238.1:n.4797+8153_4797+8155dup
NR_163239.1:n.4977_4979dup
NM_001379081.2:c.4222_4224dup MANE Select	NP_001366010.1:p.Asp1408_Arg1409insAsp
NM_144966.7:c.4222_4224dup	NP_659403.4:p.Asp1408_Arg1409insAsp
NR_163238.2:n.4797+8153_4797+8155dup
NR_163239.2:n.4977_4979dup