Canonical Allele Identifier: CA12033104
Gene: FER HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.109166792G>A , CM000667.2:g.109166792G>A GRCh38
NC_000005.9:g.108502493G>A , CM000667.1:g.108502493G>A GRCh37
NC_000005.8:g.108530392G>A NCBI36
NG_011445.2:g.423971G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281092.9:c.2049-13955G>A MANE Select ENSP00000281092.4:n.2049-13955G>A
ENST00000281092.8:c.2049-13955G>A ENSP00000281092.4:n.2049-13955G>A
ENST00000438717.6:c.816-13955G>A ENSP00000394297.4:n.816-13955G>A
ENST00000504143.6:c.*1520-13955G>A ENSP00000421951.2:n.*1520-13955G>A
ENST00000618353.1:c.942-13955G>A ENSP00000484767.1:n.942-13955G>A
NM_001308028.1:c.1524-13955G>A NP_001294957.1:n.1524-13955G>A
NM_001308031.1:c.942-13955G>A NP_001294960.1:n.942-13955G>A
NM_005246.2:c.2049-13955G>A NP_005237.2:n.2049-13955G>A
NM_005246.3:c.2049-13955G>A NP_005237.2:n.2049-13955G>A
XM_011543266.1:c.2094-13955G>A XP_011541568.1:n.2094-13955G>A
XM_011543267.1:c.2094-13955G>A XP_011541569.1:n.2094-13955G>A
XM_011543268.1:c.2094-13955G>A XP_011541570.1:n.2094-13955G>A
XM_011543269.1:c.2094-13955G>A XP_011541571.1:n.2094-13955G>A
XM_011543270.1:c.2094-13955G>A XP_011541572.1:n.2094-13955G>A
XM_011543271.1:c.2049-13955G>A XP_011541573.1:n.2049-13955G>A
XM_011543272.1:c.1890-13955G>A XP_011541574.1:n.1890-13955G>A
XM_011543273.1:c.1875-13955G>A XP_011541575.1:n.1875-13955G>A
XM_011543274.1:c.1875-13955G>A XP_011541576.1:n.1875-13955G>A
XM_011543276.1:c.987-13955G>A XP_011541578.1:n.987-13955G>A
XR_948244.1:n.2451+12424G>A
XR_948655.1:n.206+37C>T
NR_146155.1:n.2345-13955G>A
XM_011543266.2:c.2094-13955G>A XP_011541568.1:n.2094-13955G>A
XM_011543267.2:c.2094-13955G>A XP_011541569.1:n.2094-13955G>A
XM_011543269.2:c.2094-13955G>A XP_011541571.1:n.2094-13955G>A
XM_011543270.3:c.2094-13955G>A XP_011541572.1:n.2094-13955G>A
XM_011543271.3:c.2049-13955G>A XP_011541573.1:n.2049-13955G>A
XM_011543272.2:c.1890-13955G>A XP_011541574.1:n.1890-13955G>A
XM_011543276.2:c.987-13955G>A XP_011541578.1:n.987-13955G>A
XM_017009229.2:c.2094-13955G>A XP_016864718.1:n.2094-13955G>A
XM_017009230.2:c.2049-13955G>A XP_016864719.1:n.2049-13955G>A
XM_017009231.2:c.2049-13955G>A XP_016864720.1:n.2049-13955G>A
XM_017009232.2:c.1902-13955G>A XP_016864721.1:n.1902-13955G>A
XM_017009233.2:c.1875-13955G>A XP_016864722.1:n.1875-13955G>A
XR_948244.2:n.2451+12424G>A
NM_005246.4:c.2049-13955G>A MANE Select NP_005237.2:n.2049-13955G>A
NM_001308028.2:c.1524-13955G>A NP_001294957.1:n.1524-13955G>A
NR_146155.2:n.2324-13955G>A
NM_001308031.2:c.942-13955G>A NP_001294960.1:n.942-13955G>A
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