Canonical Allele Identifier: CA274566621

Gene: KIF7

Linked Data

• ClinVar Variation Id: 1462165
• ClinVar RCV Id: RCV001985634
• dbSNP Id: rs935084157
• gnomAD v4: 15-89631727-C-T
• MyVariant Identifiers: chr15:g.90174958C>T (hg19) ; chr15:g.89631727C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89631727C>T , CM000677.2:g.89631727C>T	GRCh38
NC_000015.9:g.90174958C>T , CM000677.1:g.90174958C>T	GRCh37
NC_000015.8:g.87975962C>T	NCBI36
NG_030338.1:g.28725G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.3019-17G>A	ENSP00000512678.1:n.3019-17G>A
ENST00000394412.8:c.2896-17G>A MANE Select	ENSP00000377934.3:n.2896-17G>A
ENST00000677187.1:n.570-17G>A
ENST00000394412.7:c.2896-17G>A	ENSP00000377934.3:n.2896-17G>A
NM_198525.2:c.2896-17G>A	NP_940927.2:n.2896-17G>A
XM_005254902.2:c.2896-17G>A	XP_005254959.1:n.2896-17G>A
XM_011521531.1:c.3019-17G>A	XP_011519833.1:n.3019-17G>A
XM_011521532.1:c.3016-17G>A	XP_011519834.1:n.3016-17G>A
XM_011521533.1:c.3016-17G>A	XP_011519835.1:n.3016-17G>A
XM_011521534.1:c.3019-17G>A	XP_011519836.1:n.3019-17G>A
XM_011521535.1:c.3019-17G>A	XP_011519837.1:n.3019-17G>A
XM_011521536.1:c.3019-17G>A	XP_011519838.1:n.3019-17G>A
XM_011521531.2:c.3019-17G>A	XP_011519833.1:n.3019-17G>A
NM_198525.3:c.2896-17G>A MANE Select	NP_940927.2:n.2896-17G>A