Canonical Allele Identifier: CA492292459

Gene: KIF7

Linked Data

• MyVariant Identifiers: chr15:g.90174804G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89631573G>C , CM000677.2:g.89631573G>C	GRCh38
NC_000015.9:g.90174804G>C , CM000677.1:g.90174804G>C	GRCh37
NC_000015.8:g.87975808G>C	NCBI36
NG_030338.1:g.28879C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.3156C>G	ENSP00000512678.1:p.Arg1052=
ENST00000394412.8:c.3033C>G MANE Select	ENSP00000377934.3:p.Arg1011=
ENST00000677187.1:n.707C>G
ENST00000394412.7:c.3033C>G	ENSP00000377934.3:p.Arg1011=
NM_198525.2:c.3033C>G	NP_940927.2:p.Arg1011=
XM_005254902.2:c.3033C>G	XP_005254959.1:p.Arg1011=
XM_011521531.1:c.3156C>G	XP_011519833.1:p.Arg1052=
XM_011521532.1:c.3153C>G	XP_011519834.1:p.Arg1051=
XM_011521533.1:c.3153C>G	XP_011519835.1:p.Arg1051=
XM_011521534.1:c.3156C>G	XP_011519836.1:p.Arg1052=
XM_011521535.1:c.3156C>G	XP_011519837.1:p.Arg1052=
XM_011521536.1:c.3156C>G	XP_011519838.1:p.Arg1052=
XM_011521531.2:c.3156C>G	XP_011519833.1:p.Arg1052=
NM_198525.3:c.3033C>G MANE Select	NP_940927.2:p.Arg1011=