Canonical Allele Identifier: CA586236477

Gene: FREM1

Linked Data

• dbSNP Id: rs1305858794
• gnomAD v2: 9-14784661-AATC-A
• gnomAD v4: 9-14784663-AATC-A
• MyVariant Identifiers: chr9:g.14784662_14784664del (hg19) ; chr9:g.14784664_14784666del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.14784666_14784668del , CM000671.2:g.14784666_14784668del	GRCh38
NC_000009.11:g.14784664_14784666del , CM000671.1:g.14784664_14784666del	GRCh37
NC_000009.10:g.14774664_14774666del	NCBI36
NG_017005.2:g.130571_130573del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380880.4:c.4178-32_4178-30del MANE Select	ENSP00000370262.3:n.4178-32_4178-30del
ENST00000380875.7:c.3981+8077_3981+8079del	ENSP00000370257.3:n.3981+8077_3981+8079del
ENST00000380880.3:c.4178-32_4178-30del	ENSP00000370262.3:n.4178-32_4178-30del
ENST00000422223.6:c.4178-32_4178-30del	ENSP00000412940.2:n.4178-32_4178-30del
ENST00000466679.1:n.208-32_208-30del
ENST00000497634.2:n.339-32_339-30del
NM_144966.5:c.4178-32_4178-30del	NP_659403.4:n.4178-32_4178-30del
XM_005251382.2:c.4178-32_4178-30del	XP_005251439.1:n.4178-32_4178-30del
XM_006716726.2:c.4178-32_4178-30del	XP_006716789.1:n.4178-32_4178-30del
XM_011517748.1:c.4178-32_4178-30del	XP_011516050.1:n.4178-32_4178-30del
XM_011517749.1:c.4178-32_4178-30del	XP_011516051.1:n.4178-32_4178-30del
XM_011517750.1:c.4178-32_4178-30del	XP_011516052.1:n.4178-32_4178-30del
XM_011517751.1:c.4178-32_4178-30del	XP_011516053.1:n.4178-32_4178-30del
XM_011517752.1:c.4178-32_4178-30del	XP_011516054.1:n.4178-32_4178-30del
XM_011517753.1:c.4178-32_4178-30del	XP_011516055.1:n.4178-32_4178-30del
XM_011517754.1:c.4178-32_4178-30del	XP_011516056.1:n.4178-32_4178-30del
XM_011517755.1:c.4178-32_4178-30del	XP_011516057.1:n.4178-32_4178-30del
XM_011517756.1:c.4178-32_4178-30del	XP_011516058.1:n.4178-32_4178-30del
XR_929188.1:n.4964-32_4964-30del
XR_929190.1:n.5067-32_5067-30del
XR_929487.1:n.89+4649_89+4651del
XM_005251382.4:c.4178-32_4178-30del	XP_005251439.1:n.4178-32_4178-30del
XM_005251384.4:c.-268-32_-268-30del	XP_005251441.1:n.-268-32_-268-30del
XM_006716729.3:c.-265-32_-265-30del	XP_006716792.1:n.-265-32_-265-30del
XM_017014316.2:c.4205-32_4205-30del	XP_016869805.1:n.4205-32_4205-30del
XM_017014317.1:c.4205-32_4205-30del	XP_016869806.1:n.4205-32_4205-30del
XM_017014319.2:c.4205-32_4205-30del	XP_016869808.1:n.4205-32_4205-30del
XM_017014320.2:c.4205-32_4205-30del	XP_016869809.1:n.4205-32_4205-30del
XM_017014321.2:c.4205-32_4205-30del	XP_016869810.1:n.4205-32_4205-30del
XM_017014322.1:c.4205-32_4205-30del	XP_016869811.1:n.4205-32_4205-30del
XM_017014323.1:c.4205-32_4205-30del	XP_016869812.1:n.4205-32_4205-30del
XM_017014324.2:c.4205-32_4205-30del	XP_016869813.1:n.4205-32_4205-30del
XM_017014325.2:c.4205-32_4205-30del	XP_016869814.1:n.4205-32_4205-30del
XM_017014326.1:c.3797-32_3797-30del	XP_016869815.1:n.3797-32_3797-30del
XM_017014327.2:c.3281-32_3281-30del	XP_016869816.1:n.3281-32_3281-30del
XM_017014328.2:c.4205-32_4205-30del	XP_016869817.1:n.4205-32_4205-30del
XM_017014329.2:c.4205-32_4205-30del	XP_016869818.1:n.4205-32_4205-30del
XR_001746194.2:n.4991-32_4991-30del
XR_001746195.2:n.4991-32_4991-30del
XR_001746196.2:n.5094-32_5094-30del
XR_001746197.2:n.4987-32_4987-30del
NR_163238.1:n.4797+8077_4797+8079del
NR_163239.1:n.4933-32_4933-30del
NM_001379081.2:c.4178-32_4178-30del MANE Select	NP_001366010.1:n.4178-32_4178-30del
NM_144966.7:c.4178-32_4178-30del	NP_659403.4:n.4178-32_4178-30del
NR_163238.2:n.4797+8077_4797+8079del
NR_163239.2:n.4933-32_4933-30del