Canonical Allele Identifier: CA165947414
Gene: FEZF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.122303578G>A , CM000669.2:g.122303578G>A GRCh38
NC_000007.13:g.121943632G>A , CM000669.1:g.121943632G>A GRCh37
NC_000007.12:g.121730868G>A NCBI36
NG_041775.1:g.5934C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000442488.7:c.801+59C>T MANE Select ENSP00000411145.2:n.801+59C>T
ENST00000427185.2:c.651+59C>T ENSP00000392727.2:n.651+59C>T
ENST00000442488.6:c.801+59C>T ENSP00000411145.2:n.801+59C>T
NM_001024613.3:c.801+59C>T NP_001019784.2:n.801+59C>T
NM_001160264.2:c.651+59C>T NP_001153736.1:n.651+59C>T
XM_005250337.2:c.801+59C>T XP_005250394.1:n.801+59C>T
XM_011516200.1:c.801+59C>T XP_011514502.1:n.801+59C>T
XM_011516201.1:c.801+59C>T XP_011514503.1:n.801+59C>T
XM_011516202.1:c.651+59C>T XP_011514504.1:n.651+59C>T
XM_005250337.3:c.801+59C>T XP_005250394.1:n.801+59C>T
XM_011516202.2:c.651+59C>T XP_011514504.1:n.651+59C>T
NM_001024613.4:c.801+59C>T MANE Select NP_001019784.2:n.801+59C>T