Canonical Allele Identifier: CA1739543409
Community Standard Title: NM_001024613.4(FEZF1):c.1070-210T=
Gene: FEZF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.122302565A= , CM000669.2:g.122302565A= GRCh38
NC_000007.13:g.121942619A= , CM000669.1:g.121942619A= GRCh37
NC_000007.12:g.121729855A= NCBI36
NG_041775.1:g.6947T=

Transcript Alleles

HGVS Amino-acid Change
NM_001024613.4:c.1070-210T= MANE Select NP_001019784.2:n.1070-210T=
ENST00000442488.7:c.1070-210T= MANE Select ENSP00000411145.2:n.1070-210T=
NM_001024613.3:c.1070-210T= NP_001019784.2:n.1070-210T=
NM_001160264.2:c.920-210T= NP_001153736.1:n.920-210T=
ENST00000427185.2:c.920-210T= ENSP00000392727.2:n.920-210T=
ENST00000442488.6:c.1070-210T= ENSP00000411145.2:n.1070-210T=
XM_005250337.2:c.1070-210T= XP_005250394.1:n.1070-210T=
XM_005250337.3:c.1070-210T= XP_005250394.1:n.1070-210T=
XM_011516200.1:c.1070-210T= XP_011514502.1:n.1070-210T=
XM_011516201.1:c.1070-210T= XP_011514503.1:n.1070-210T=
XM_011516202.1:c.920-210T= XP_011514504.1:n.920-210T=
XM_011516202.2:c.920-210T= XP_011514504.1:n.920-210T=