Canonical Allele Identifier: CA2649720755

Gene: KIF14

Linked Data

• gnomAD v4: 1-200603834-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200603834T>C , CM000663.2:g.200603834T>C	GRCh38
NC_000001.10:g.200572962T>C , CM000663.1:g.200572962T>C	GRCh37
NC_000001.9:g.198839585T>C	NCBI36
NG_042074.1:g.21901A>G

Transcript Alleles

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