Canonical Allele Identifier: CA2649720749
Gene: KIF14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.200603827C>T , CM000663.2:g.200603827C>T GRCh38
NC_000001.10:g.200572955C>T , CM000663.1:g.200572955C>T GRCh37
NC_000001.9:g.198839578C>T NCBI36
NG_042074.1:g.21908G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367350.5:c.1863+12G>A MANE Select ENSP00000356319.4:n.1863+12G>A
ENST00000367350.4:c.1863+12G>A ENSP00000356319.4:n.1863+12G>A
ENST00000614960.4:c.1863+12G>A ENSP00000483069.1:n.1863+12G>A
NM_001305792.1:c.390+12G>A NP_001292721.1:n.390+12G>A
NM_014875.2:c.1863+12G>A NP_055690.1:n.1863+12G>A
XM_011510230.1:c.1863+12G>A XP_011508532.1:n.1863+12G>A
XM_011510231.1:c.1863+12G>A XP_011508533.1:n.1863+12G>A
XM_011510232.1:c.1863+12G>A XP_011508534.1:n.1863+12G>A
XM_011510233.1:c.1779+12G>A XP_011508535.1:n.1779+12G>A
XM_011510234.1:c.1764+12G>A XP_011508536.1:n.1764+12G>A
XM_011510235.1:c.1491+12G>A XP_011508537.1:n.1491+12G>A
XM_011510236.1:c.390+12G>A XP_011508538.1:n.390+12G>A
XM_011510231.2:c.1863+12G>A XP_011508533.1:n.1863+12G>A
XM_011510232.2:c.1863+12G>A XP_011508534.1:n.1863+12G>A
XM_011510233.2:c.1779+12G>A XP_011508535.1:n.1779+12G>A
XM_011510235.2:c.1491+12G>A XP_011508537.1:n.1491+12G>A
XM_017003005.1:c.1863+12G>A XP_016858494.1:n.1863+12G>A
XM_017003006.1:c.1734+12G>A XP_016858495.1:n.1734+12G>A
XM_017003007.1:c.1296+12G>A XP_016858496.1:n.1296+12G>A
NM_014875.3:c.1863+12G>A MANE Select NP_055690.1:n.1863+12G>A