Canonical Allele Identifier: CA1835222385

Gene: FREM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.14842476G= , CM000671.2:g.14842476G=	GRCh38
NC_000009.11:g.14842474G= , CM000671.1:g.14842474G=	GRCh37
NC_000009.10:g.14832474G=	NCBI36
NG_017005.2:g.72761C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380880.4:c.1578C= MANE Select	ENSP00000370262.3:p.Thr526=
ENST00000380875.7:c.1578C=	ENSP00000370257.3:p.Thr526=
ENST00000380880.3:c.1578C=	ENSP00000370262.3:p.Thr526=
ENST00000422223.6:c.1578C=	ENSP00000412940.2:p.Thr526=
NM_144966.5:c.1578C=	NP_659403.4:p.Thr526=
XM_005251382.2:c.1578C=	XP_005251439.1:p.Thr526=
XM_006716726.2:c.1578C=	XP_006716789.1:p.Thr526=
XM_006716728.2:c.1578C=	XP_006716791.1:p.Thr526=
XM_011517748.1:c.1578C=	XP_011516050.1:p.Thr526=
XM_011517749.1:c.1578C=	XP_011516051.1:p.Thr526=
XM_011517750.1:c.1578C=	XP_011516052.1:p.Thr526=
XM_011517751.1:c.1578C=	XP_011516053.1:p.Thr526=
XM_011517752.1:c.1578C=	XP_011516054.1:p.Thr526=
XM_011517753.1:c.1578C=	XP_011516055.1:p.Thr526=
XM_011517754.1:c.1578C=	XP_011516056.1:p.Thr526=
XM_011517755.1:c.1578C=	XP_011516057.1:p.Thr526=
XM_011517756.1:c.1578C=	XP_011516058.1:p.Thr526=
XM_011517757.1:c.1578C=	XP_011516059.1:p.Thr526=
XR_929188.1:n.2364C=
XR_929190.1:n.2364C=
XM_005251382.4:c.1578C=	XP_005251439.1:p.Thr526=
XM_017014316.2:c.1605C=	XP_016869805.1:p.Thr535=
XM_017014317.1:c.1605C=	XP_016869806.1:p.Thr535=
XM_017014319.2:c.1605C=	XP_016869808.1:p.Thr535=
XM_017014320.2:c.1605C=	XP_016869809.1:p.Thr535=
XM_017014321.2:c.1605C=	XP_016869810.1:p.Thr535=
XM_017014322.1:c.1605C=	XP_016869811.1:p.Thr535=
XM_017014323.1:c.1605C=	XP_016869812.1:p.Thr535=
XM_017014324.2:c.1605C=	XP_016869813.1:p.Thr535=
XM_017014325.2:c.1605C=	XP_016869814.1:p.Thr535=
XM_017014326.1:c.1197C=	XP_016869815.1:p.Thr399=
XM_017014327.2:c.681C=	XP_016869816.1:p.Thr227=
XM_017014328.2:c.1605C=	XP_016869817.1:p.Thr535=
XM_017014329.2:c.1605C=	XP_016869818.1:p.Thr535=
XM_017014330.2:c.1605C=	XP_016869819.1:p.Thr535=
XR_001746194.2:n.2391C=
XR_001746195.2:n.2391C=
XR_001746196.2:n.2391C=
XR_001746197.2:n.2391C=
NR_163238.1:n.2394C=
NR_163239.1:n.2338C=
NM_001379081.2:c.1578C= MANE Select	NP_001366010.1:p.Thr526=
NM_144966.7:c.1578C=	NP_659403.4:p.Thr526=
NR_163238.2:n.2394C=
NR_163239.2:n.2338C=