Canonical Allele Identifier: CA344101729

Gene: KIF14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200606783G>C , CM000663.2:g.200606783G>C	GRCh38
NC_000001.10:g.200575911G>C , CM000663.1:g.200575911G>C	GRCh37
NC_000001.9:g.198842534G>C	NCBI36
NG_042074.1:g.18952C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014875.3:c.1570C>G MANE Select	NP_055690.1:p.His524Asp
ENST00000367350.5:c.1570C>G MANE Select	ENSP00000356319.4:p.His524Asp
NM_001305792.1:c.97C>G	NP_001292721.1:p.His33Asp
NM_014875.2:c.1570C>G	NP_055690.1:p.His524Asp
ENST00000367350.4:c.1570C>G	ENSP00000356319.4:p.His524Asp
ENST00000614960.4:c.1570C>G	ENSP00000483069.1:p.His524Asp
XM_011510230.1:c.1570C>G	XP_011508532.1:p.His524Asp
XM_011510231.1:c.1570C>G	XP_011508533.1:p.His524Asp
XM_011510231.2:c.1570C>G	XP_011508533.1:p.His524Asp
XM_011510232.1:c.1570C>G	XP_011508534.1:p.His524Asp
XM_011510232.2:c.1570C>G	XP_011508534.1:p.His524Asp
XM_011510233.1:c.1486C>G	XP_011508535.1:p.His496Asp
XM_011510233.2:c.1486C>G	XP_011508535.1:p.His496Asp
XM_011510234.1:c.1471C>G	XP_011508536.1:p.His491Asp
XM_011510235.1:c.1198C>G	XP_011508537.1:p.His400Asp
XM_011510235.2:c.1198C>G	XP_011508537.1:p.His400Asp
XM_011510236.1:c.97C>G	XP_011508538.1:p.His33Asp
XM_017003005.1:c.1570C>G	XP_016858494.1:p.His524Asp
XM_017003006.1:c.1441C>G	XP_016858495.1:p.His481Asp
XM_017003007.1:c.1003C>G	XP_016858496.1:p.His335Asp