Canonical Allele Identifier: CA1835190768
Gene: FREM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.14784618A= , CM000671.2:g.14784618A= GRCh38
NC_000009.11:g.14784616A= , CM000671.1:g.14784616A= GRCh37
NC_000009.10:g.14774616A= NCBI36
NG_017005.2:g.130619T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380880.4:c.4194T= MANE Select ENSP00000370262.3:p.Leu1398=
ENST00000380875.7:c.3981+8125T= ENSP00000370257.3:n.3981+8125T=
ENST00000380880.3:c.4194T= ENSP00000370262.3:p.Leu1398=
ENST00000422223.6:c.4194T= ENSP00000412940.2:p.Leu1398=
ENST00000466679.1:n.224T=
ENST00000485068.5:n.17T=
ENST00000497634.2:n.355T=
NM_144966.5:c.4194T= NP_659403.4:p.Leu1398=
XM_005251382.2:c.4194T= XP_005251439.1:p.Leu1398=
XM_006716726.2:c.4194T= XP_006716789.1:p.Leu1398=
XM_011517748.1:c.4194T= XP_011516050.1:p.Leu1398=
XM_011517749.1:c.4194T= XP_011516051.1:p.Leu1398=
XM_011517750.1:c.4194T= XP_011516052.1:p.Leu1398=
XM_011517751.1:c.4194T= XP_011516053.1:p.Leu1398=
XM_011517752.1:c.4194T= XP_011516054.1:p.Leu1398=
XM_011517753.1:c.4194T= XP_011516055.1:p.Leu1398=
XM_011517754.1:c.4194T= XP_011516056.1:p.Leu1398=
XM_011517755.1:c.4194T= XP_011516057.1:p.Leu1398=
XM_011517756.1:c.4194T= XP_011516058.1:p.Leu1398=
XR_929188.1:n.4980T=
XR_929190.1:n.5083T=
XR_929487.1:n.89+4601A=
XM_005251382.4:c.4194T= XP_005251439.1:p.Leu1398=
XM_005251384.4:c.-252T= XP_005251441.1:n.-252T=
XM_006716729.3:c.-249T= XP_006716792.1:n.-249T=
XM_017014316.2:c.4221T= XP_016869805.1:p.Leu1407=
XM_017014317.1:c.4221T= XP_016869806.1:p.Leu1407=
XM_017014319.2:c.4221T= XP_016869808.1:p.Leu1407=
XM_017014320.2:c.4221T= XP_016869809.1:p.Leu1407=
XM_017014321.2:c.4221T= XP_016869810.1:p.Leu1407=
XM_017014322.1:c.4221T= XP_016869811.1:p.Leu1407=
XM_017014323.1:c.4221T= XP_016869812.1:p.Leu1407=
XM_017014324.2:c.4221T= XP_016869813.1:p.Leu1407=
XM_017014325.2:c.4221T= XP_016869814.1:p.Leu1407=
XM_017014326.1:c.3813T= XP_016869815.1:p.Leu1271=
XM_017014327.2:c.3297T= XP_016869816.1:p.Leu1099=
XM_017014328.2:c.4221T= XP_016869817.1:p.Leu1407=
XM_017014329.2:c.4221T= XP_016869818.1:p.Leu1407=
XR_001746194.2:n.5007T=
XR_001746195.2:n.5007T=
XR_001746196.2:n.5110T=
XR_001746197.2:n.5003T=
NR_163238.1:n.4797+8125T=
NR_163239.1:n.4949T=
NM_001379081.2:c.4194T= MANE Select NP_001366010.1:p.Leu1398=
NM_144966.7:c.4194T= NP_659403.4:p.Leu1398=
NR_163238.2:n.4797+8125T=
NR_163239.2:n.4949T=