Canonical Allele Identifier: CA7727839

Gene: KIF7

Linked Data

• ClinVar Variation Id: 1562655
• ClinVar RCV Id: RCV002204954
• dbSNP Id: rs141683648
• ExAC: 15:90174762 G / A
• gnomAD v2: 15-90174762-G-A
• gnomAD v3: 15-89631531-G-A
• gnomAD v4: 15-89631531-G-A
• MyVariant Identifiers: chr15:g.90174762G>A (hg19) ; chr15:g.89631531G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89631531G>A , CM000677.2:g.89631531G>A	GRCh38
NC_000015.9:g.90174762G>A , CM000677.1:g.90174762G>A	GRCh37
NC_000015.8:g.87975766G>A	NCBI36
NG_030338.1:g.28921C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696512.1:c.3198C>T	ENSP00000512678.1:p.Asp1066=
ENST00000394412.8:c.3075C>T MANE Select	ENSP00000377934.3:p.Asp1025=
ENST00000677187.1:n.749C>T
ENST00000394412.7:c.3075C>T	ENSP00000377934.3:p.Asp1025=
NM_198525.2:c.3075C>T	NP_940927.2:p.Asp1025=
XM_005254902.2:c.3075C>T	XP_005254959.1:p.Asp1025=
XM_011521531.1:c.3198C>T	XP_011519833.1:p.Asp1066=
XM_011521532.1:c.3195C>T	XP_011519834.1:p.Asp1065=
XM_011521533.1:c.3195C>T	XP_011519835.1:p.Asp1065=
XM_011521534.1:c.3198C>T	XP_011519836.1:p.Asp1066=
XM_011521535.1:c.3198C>T	XP_011519837.1:p.Asp1066=
XM_011521536.1:c.3198C>T	XP_011519838.1:p.Asp1066=
XM_011521531.2:c.3198C>T	XP_011519833.1:p.Asp1066=
NM_198525.3:c.3075C>T MANE Select	NP_940927.2:p.Asp1025=