Canonical Allele Identifier: CA393755872

Gene: KIF7 TICRR

Linked Data

• ClinVar Variation Id: 451951
• ClinVar RCV Id: RCV000522960 ; RCV001381328
• dbSNP Id: rs1555423165
• MyVariant Identifiers: chr15:g.90173555G>C (hg19) ; chr15:g.89630324G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89630324G>C , CM000677.2:g.89630324G>C	GRCh38
NC_000015.9:g.90173555G>C , CM000677.1:g.90173555G>C	GRCh37
NC_000015.8:g.87974559G>C	NCBI36
NG_030338.1:g.30128C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.3404C>G (KIF7)	ENSP00000512678.1:p.Ser1135Ter
ENST00000394412.8:c.3281C>G (KIF7) MANE Select	ENSP00000377934.3:p.Ser1094Ter
ENST00000677187.1:n.955C>G (KIF7)
ENST00000394412.7:c.3281C>G (KIF7)	ENSP00000377934.3:p.Ser1094Ter
ENST00000561095.1:c.1635G>C (TICRR)
NM_198525.2:c.3281C>G (KIF7)	NP_940927.2:p.Ser1094Ter
XM_005254902.2:c.3281C>G (KIF7)	XP_005254959.1:p.Ser1094Ter
XM_011521531.1:c.3404C>G (KIF7)	XP_011519833.1:p.Ser1135Ter
XM_011521532.1:c.3401C>G (KIF7)	XP_011519834.1:p.Ser1134Ter
XM_011521533.1:c.3401C>G (KIF7)	XP_011519835.1:p.Ser1134Ter
XM_011521534.1:c.3404C>G (KIF7)	XP_011519836.1:p.Ser1135Ter
XM_011521535.1:c.3404C>G (KIF7)	XP_011519837.1:p.Ser1135Ter
XM_011521536.1:c.3404C>G (KIF7)	XP_011519838.1:p.Ser1135Ter
XM_011521531.2:c.3404C>G (KIF7)	XP_011519833.1:p.Ser1135Ter
NM_198525.3:c.3281C>G (KIF7) MANE Select	NP_940927.2:p.Ser1094Ter