Canonical Allele Identifier: CA7727893

Gene: KIF7

Linked Data

• dbSNP Id: rs769595008
• ExAC: 15:90174965 T / G
• gnomAD v4: 15-89631734-T-G
• MyVariant Identifiers: chr15:g.90174965T>G (hg19) ; chr15:g.89631734T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89631734T>G , CM000677.2:g.89631734T>G	GRCh38
NC_000015.9:g.90174965T>G , CM000677.1:g.90174965T>G	GRCh37
NC_000015.8:g.87975969T>G	NCBI36
NG_030338.1:g.28718A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.3019-24A>C	ENSP00000512678.1:n.3019-24A>C
ENST00000394412.8:c.2896-24A>C MANE Select	ENSP00000377934.3:n.2896-24A>C
ENST00000677187.1:n.570-24A>C
ENST00000394412.7:c.2896-24A>C	ENSP00000377934.3:n.2896-24A>C
NM_198525.2:c.2896-24A>C	NP_940927.2:n.2896-24A>C
XM_005254902.2:c.2896-24A>C	XP_005254959.1:n.2896-24A>C
XM_011521531.1:c.3019-24A>C	XP_011519833.1:n.3019-24A>C
XM_011521532.1:c.3016-24A>C	XP_011519834.1:n.3016-24A>C
XM_011521533.1:c.3016-24A>C	XP_011519835.1:n.3016-24A>C
XM_011521534.1:c.3019-24A>C	XP_011519836.1:n.3019-24A>C
XM_011521535.1:c.3019-24A>C	XP_011519837.1:n.3019-24A>C
XM_011521536.1:c.3019-24A>C	XP_011519838.1:n.3019-24A>C
XM_011521531.2:c.3019-24A>C	XP_011519833.1:n.3019-24A>C
NM_198525.3:c.2896-24A>C MANE Select	NP_940927.2:n.2896-24A>C