Canonical Allele Identifier: CA4458865

Gene: FEZF1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.122302793G>C , CM000669.2:g.122302793G>C	GRCh38
NC_000007.13:g.121942847G>C , CM000669.1:g.121942847G>C	GRCh37
NC_000007.12:g.121730083G>C	NCBI36
NG_041775.1:g.6719C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001024613.4:c.1069+6C>G MANE Select	NP_001019784.2:n.1069+6C>G
ENST00000442488.7:c.1069+6C>G MANE Select	ENSP00000411145.2:n.1069+6C>G
NM_001024613.3:c.1069+6C>G	NP_001019784.2:n.1069+6C>G
NM_001160264.2:c.919+6C>G	NP_001153736.1:n.919+6C>G
ENST00000427185.2:c.919+6C>G	ENSP00000392727.2:n.919+6C>G
ENST00000442488.6:c.1069+6C>G	ENSP00000411145.2:n.1069+6C>G
XM_005250337.2:c.1069+6C>G	XP_005250394.1:n.1069+6C>G
XM_005250337.3:c.1069+6C>G	XP_005250394.1:n.1069+6C>G
XM_011516200.1:c.1069+6C>G	XP_011514502.1:n.1069+6C>G
XM_011516201.1:c.1069+6C>G	XP_011514503.1:n.1069+6C>G
XM_011516202.1:c.919+6C>G	XP_011514504.1:n.919+6C>G
XM_011516202.2:c.919+6C>G	XP_011514504.1:n.919+6C>G