Canonical Allele Identifier: CA1835190670

Gene: FREM1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.14784446_14784447delinsTG , CM000671.2:g.14784446_14784447delinsTG	GRCh38
NC_000009.11:g.14784444_14784445delinsTG , CM000671.1:g.14784444_14784445delinsTG	GRCh37
NC_000009.10:g.14774444_14774445delinsTG	NCBI36
NG_017005.2:g.130790_130791delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380880.4:c.4365_4366delinsCA MANE Select	ENSP00000370262.3:p.Phe1455=
ENST00000380875.7:c.3981+8296_3981+8297delinsCA	ENSP00000370257.3:n.3981+8296_3981+8297delinsCA
ENST00000380880.3:c.4365_4366delinsCA	ENSP00000370262.3:p.Phe1455=
ENST00000422223.6:c.4365_4366delinsCA	ENSP00000412940.2:p.Phe1455=
ENST00000466679.1:n.395_396delinsCA
ENST00000485068.5:n.188_189delinsCA
ENST00000497634.2:n.526_527delinsCA
NM_144966.5:c.4365_4366delinsCA	NP_659403.4:p.Phe1455=
XM_005251382.2:c.4365_4366delinsCA	XP_005251439.1:p.Phe1455=
XM_005251384.3:c.-81_-80delinsCA	XP_005251441.1:n.-81_-80delinsCA
XM_006716726.2:c.4365_4366delinsCA	XP_006716789.1:p.Phe1455=
XM_006716729.2:c.-78_-77delinsCA	XP_006716792.1:n.-78_-77delinsCA
XM_011517748.1:c.4365_4366delinsCA	XP_011516050.1:p.Phe1455=
XM_011517749.1:c.4365_4366delinsCA	XP_011516051.1:p.Phe1455=
XM_011517750.1:c.4365_4366delinsCA	XP_011516052.1:p.Phe1455=
XM_011517751.1:c.4365_4366delinsCA	XP_011516053.1:p.Phe1455=
XM_011517752.1:c.4365_4366delinsCA	XP_011516054.1:p.Phe1455=
XM_011517753.1:c.4365_4366delinsCA	XP_011516055.1:p.Phe1455=
XM_011517754.1:c.4365_4366delinsCA	XP_011516056.1:p.Phe1455=
XM_011517755.1:c.4365_4366delinsCA	XP_011516057.1:p.Phe1455=
XM_011517756.1:c.4365_4366delinsCA	XP_011516058.1:p.Phe1455=
XR_929188.1:n.5151_5152delinsCA
XR_929487.1:n.89+4429_89+4430delinsTG
XM_005251382.4:c.4365_4366delinsCA	XP_005251439.1:p.Phe1455=
XM_005251384.4:c.-81_-80delinsCA	XP_005251441.1:n.-81_-80delinsCA
XM_006716729.3:c.-78_-77delinsCA	XP_006716792.1:n.-78_-77delinsCA
XM_017014316.2:c.4392_4393delinsCA	XP_016869805.1:p.Phe1464=
XM_017014317.1:c.4392_4393delinsCA	XP_016869806.1:p.Phe1464=
XM_017014319.2:c.4392_4393delinsCA	XP_016869808.1:p.Phe1464=
XM_017014320.2:c.4392_4393delinsCA	XP_016869809.1:p.Phe1464=
XM_017014321.2:c.4392_4393delinsCA	XP_016869810.1:p.Phe1464=
XM_017014322.1:c.4392_4393delinsCA	XP_016869811.1:p.Phe1464=
XM_017014323.1:c.4392_4393delinsCA	XP_016869812.1:p.Phe1464=
XM_017014324.2:c.4392_4393delinsCA	XP_016869813.1:p.Phe1464=
XM_017014325.2:c.4392_4393delinsCA	XP_016869814.1:p.Phe1464=
XM_017014326.1:c.3984_3985delinsCA	XP_016869815.1:p.Phe1328=
XM_017014327.2:c.3468_3469delinsCA	XP_016869816.1:p.Phe1156=
XM_017014328.2:c.4392_4393delinsCA	XP_016869817.1:p.Phe1464=
XM_017014329.2:c.4392_4393delinsCA	XP_016869818.1:p.Phe1464=
XR_001746194.2:n.5178_5179delinsCA
XR_001746195.2:n.5178_5179delinsCA
XR_001746197.2:n.5174_5175delinsCA
NR_163238.1:n.4797+8296_4797+8297delinsCA
NR_163239.1:n.5120_5121delinsCA
NM_001379081.2:c.4365_4366delinsCA MANE Select	NP_001366010.1:p.Phe1455=
NM_144966.7:c.4365_4366delinsCA	NP_659403.4:p.Phe1455=
NR_163238.2:n.4797+8296_4797+8297delinsCA
NR_163239.2:n.5120_5121delinsCA