Canonical Allele Identifier: CA372966322

Gene: FREM1

Linked Data

• dbSNP Id: rs200573582
• gnomAD v4: 9-14784574-G-A
• MyVariant Identifiers: chr9:g.14784572G>A (hg19) ; chr9:g.14784574G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.14784574G>A , CM000671.2:g.14784574G>A	GRCh38
NC_000009.11:g.14784572G>A , CM000671.1:g.14784572G>A	GRCh37
NC_000009.10:g.14774572G>A	NCBI36
NG_017005.2:g.130663C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380880.4:c.4238C>T MANE Select	ENSP00000370262.3:p.Thr1413Ile
ENST00000380875.7:c.3981+8169C>T	ENSP00000370257.3:n.3981+8169C>T
ENST00000380880.3:c.4238C>T	ENSP00000370262.3:p.Thr1413Ile
ENST00000422223.6:c.4238C>T	ENSP00000412940.2:p.Thr1413Ile
ENST00000466679.1:n.268C>T
ENST00000485068.5:n.61C>T
ENST00000497634.2:n.399C>T
NM_144966.5:c.4238C>T	NP_659403.4:p.Thr1413Ile
XM_005251382.2:c.4238C>T	XP_005251439.1:p.Thr1413Ile
XM_006716726.2:c.4238C>T	XP_006716789.1:p.Thr1413Ile
XM_011517748.1:c.4238C>T	XP_011516050.1:p.Thr1413Ile
XM_011517749.1:c.4238C>T	XP_011516051.1:p.Thr1413Ile
XM_011517750.1:c.4238C>T	XP_011516052.1:p.Thr1413Ile
XM_011517751.1:c.4238C>T	XP_011516053.1:p.Thr1413Ile
XM_011517752.1:c.4238C>T	XP_011516054.1:p.Thr1413Ile
XM_011517753.1:c.4238C>T	XP_011516055.1:p.Thr1413Ile
XM_011517754.1:c.4238C>T	XP_011516056.1:p.Thr1413Ile
XM_011517755.1:c.4238C>T	XP_011516057.1:p.Thr1413Ile
XM_011517756.1:c.4238C>T	XP_011516058.1:p.Thr1413Ile
XR_929188.1:n.5024C>T
XR_929190.1:n.5127C>T
XR_929487.1:n.89+4557G>A
XM_005251382.4:c.4238C>T	XP_005251439.1:p.Thr1413Ile
XM_005251384.4:c.-208C>T	XP_005251441.1:n.-208C>T
XM_006716729.3:c.-205C>T	XP_006716792.1:n.-205C>T
XM_017014316.2:c.4265C>T	XP_016869805.1:p.Thr1422Ile
XM_017014317.1:c.4265C>T	XP_016869806.1:p.Thr1422Ile
XM_017014319.2:c.4265C>T	XP_016869808.1:p.Thr1422Ile
XM_017014320.2:c.4265C>T	XP_016869809.1:p.Thr1422Ile
XM_017014321.2:c.4265C>T	XP_016869810.1:p.Thr1422Ile
XM_017014322.1:c.4265C>T	XP_016869811.1:p.Thr1422Ile
XM_017014323.1:c.4265C>T	XP_016869812.1:p.Thr1422Ile
XM_017014324.2:c.4265C>T	XP_016869813.1:p.Thr1422Ile
XM_017014325.2:c.4265C>T	XP_016869814.1:p.Thr1422Ile
XM_017014326.1:c.3857C>T	XP_016869815.1:p.Thr1286Ile
XM_017014327.2:c.3341C>T	XP_016869816.1:p.Thr1114Ile
XM_017014328.2:c.4265C>T	XP_016869817.1:p.Thr1422Ile
XM_017014329.2:c.4265C>T	XP_016869818.1:p.Thr1422Ile
XR_001746194.2:n.5051C>T
XR_001746195.2:n.5051C>T
XR_001746196.2:n.5154C>T
XR_001746197.2:n.5047C>T
NR_163238.1:n.4797+8169C>T
NR_163239.1:n.4993C>T
NM_001379081.2:c.4238C>T MANE Select	NP_001366010.1:p.Thr1413Ile
NM_144966.7:c.4238C>T	NP_659403.4:p.Thr1413Ile
NR_163238.2:n.4797+8169C>T
NR_163239.2:n.4993C>T