Canonical Allele Identifier: CA7728267

Gene: KIF7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89642378T>C , CM000677.2:g.89642378T>C	GRCh38
NC_000015.9:g.90185609T>C , CM000677.1:g.90185609T>C	GRCh37
NC_000015.8:g.87986613T>C	NCBI36
NG_030338.1:g.18074A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.2342A>G	ENSP00000512678.1:p.Gln781Arg
ENST00000394412.8:c.2219A>G MANE Select	ENSP00000377934.3:p.Gln740Arg
ENST00000394412.7:c.2219A>G	ENSP00000377934.3:p.Gln740Arg
NM_198525.2:c.2219A>G	NP_940927.2:p.Gln740Arg
XM_005254902.2:c.2219A>G	XP_005254959.1:p.Gln740Arg
XM_011521531.1:c.2342A>G	XP_011519833.1:p.Gln781Arg
XM_011521532.1:c.2339A>G	XP_011519834.1:p.Gln780Arg
XM_011521533.1:c.2339A>G	XP_011519835.1:p.Gln780Arg
XM_011521534.1:c.2342A>G	XP_011519836.1:p.Gln781Arg
XM_011521535.1:c.2342A>G	XP_011519837.1:p.Gln781Arg
XM_011521536.1:c.2342A>G	XP_011519838.1:p.Gln781Arg
XM_011521537.1:c.2342A>G	XP_011519839.1:p.Gln781Arg
XM_011521531.2:c.2342A>G	XP_011519833.1:p.Gln781Arg
NM_198525.3:c.2219A>G MANE Select	NP_940927.2:p.Gln740Arg