Canonical Allele Identifier: CA2630274216

Gene: KIF7

Linked Data

• gnomAD v4: 15-89631736-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89631736G>T , CM000677.2:g.89631736G>T	GRCh38
NC_000015.9:g.90174967G>T , CM000677.1:g.90174967G>T	GRCh37
NC_000015.8:g.87975971G>T	NCBI36
NG_030338.1:g.28716C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.3019-26C>A	ENSP00000512678.1:n.3019-26C>A
ENST00000394412.8:c.2896-26C>A MANE Select	ENSP00000377934.3:n.2896-26C>A
ENST00000677187.1:n.570-26C>A
ENST00000394412.7:c.2896-26C>A	ENSP00000377934.3:n.2896-26C>A
NM_198525.2:c.2896-26C>A	NP_940927.2:n.2896-26C>A
XM_005254902.2:c.2896-26C>A	XP_005254959.1:n.2896-26C>A
XM_011521531.1:c.3019-26C>A	XP_011519833.1:n.3019-26C>A
XM_011521532.1:c.3016-26C>A	XP_011519834.1:n.3016-26C>A
XM_011521533.1:c.3016-26C>A	XP_011519835.1:n.3016-26C>A
XM_011521534.1:c.3019-26C>A	XP_011519836.1:n.3019-26C>A
XM_011521535.1:c.3019-26C>A	XP_011519837.1:n.3019-26C>A
XM_011521536.1:c.3019-26C>A	XP_011519838.1:n.3019-26C>A
XM_011521531.2:c.3019-26C>A	XP_011519833.1:n.3019-26C>A
NM_198525.3:c.2896-26C>A MANE Select	NP_940927.2:n.2896-26C>A