Canonical Allele Identifier: CA4458928

Gene: FEZF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.122303627T>A , CM000669.2:g.122303627T>A	GRCh38
NC_000007.13:g.121943681T>A , CM000669.1:g.121943681T>A	GRCh37
NC_000007.12:g.121730917T>A	NCBI36
NG_041775.1:g.5885A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001024613.4:c.801+10A>T MANE Select	NP_001019784.2:n.801+10A>T
ENST00000442488.7:c.801+10A>T MANE Select	ENSP00000411145.2:n.801+10A>T
NM_001024613.3:c.801+10A>T	NP_001019784.2:n.801+10A>T
NM_001160264.2:c.651+10A>T	NP_001153736.1:n.651+10A>T
ENST00000427185.2:c.651+10A>T	ENSP00000392727.2:n.651+10A>T
ENST00000442488.6:c.801+10A>T	ENSP00000411145.2:n.801+10A>T
XM_005250337.2:c.801+10A>T	XP_005250394.1:n.801+10A>T
XM_005250337.3:c.801+10A>T	XP_005250394.1:n.801+10A>T
XM_011516200.1:c.801+10A>T	XP_011514502.1:n.801+10A>T
XM_011516201.1:c.801+10A>T	XP_011514503.1:n.801+10A>T
XM_011516202.1:c.651+10A>T	XP_011514504.1:n.651+10A>T
XM_011516202.2:c.651+10A>T	XP_011514504.1:n.651+10A>T