Canonical Allele Identifier: CA1622742109
Gene: KIF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39571431C= , CM000668.2:g.39571431C= GRCh38
NC_000006.11:g.39539207C= , CM000668.1:g.39539207C= GRCh37
NC_000006.10:g.39647185C= NCBI36
NG_054928.1:g.158994G=

Transcript Alleles

HGVS Amino-acid Change
NM_145027.6:c.1181+6625G= MANE Select NP_659464.3:n.1181+6625G=
ENST00000287152.12:c.1181+6625G= MANE Select ENSP00000287152.7:n.1181+6625G=
NM_001289020.1:c.1181+6625G= NP_001275949.1:n.1181+6625G=
NM_001289020.2:c.1181+6625G= NP_001275949.1:n.1181+6625G=
NM_001289020.3:c.1181+6625G= NP_001275949.1:n.1181+6625G=
NM_001289021.1:c.1181+6625G= NP_001275950.1:n.1181+6625G=
NM_001289021.2:c.1181+6625G= NP_001275950.1:n.1181+6625G=
NM_001289021.3:c.1181+6625G= NP_001275950.1:n.1181+6625G=
NM_145027.4:c.1181+6625G= NP_659464.3:n.1181+6625G=
NM_145027.5:c.1181+6625G= NP_659464.3:n.1181+6625G=
ENST00000287152.11:c.1181+6625G= ENSP00000287152.7:n.1181+6625G=
ENST00000458470.5:c.856+6625G=
ENST00000538893.5:c.-299+6625G= ENSP00000441435.2:n.-299+6625G=
XM_005248904.3:c.1181+6625G= XP_005248961.1:n.1181+6625G=
XM_005248904.4:c.1181+6625G= XP_005248961.1:n.1181+6625G=
XM_011514357.1:c.1181+6625G= XP_011512659.1:n.1181+6625G=
XM_011514357.3:c.1181+6625G= XP_011512659.1:n.1181+6625G=
XM_011514358.1:c.1181+6625G= XP_011512660.1:n.1181+6625G=
XM_011514358.3:c.1181+6625G= XP_011512660.1:n.1181+6625G=
XM_011514359.1:c.1181+6625G= XP_011512661.1:n.1181+6625G=
XM_011514359.3:c.1181+6625G= XP_011512661.1:n.1181+6625G=
XM_011514360.1:c.554+6625G= XP_011512662.1:n.554+6625G=
XM_011514361.1:c.1181+6625G= XP_011512663.1:n.1181+6625G=
XM_011514361.2:c.1181+6625G= XP_011512663.1:n.1181+6625G=
XM_017010427.1:c.872+6625G= XP_016865916.1:n.872+6625G=
XM_017010428.1:c.536+6625G= XP_016865917.1:n.536+6625G=
XR_001743238.1:n.1276+6625G=