Canonical Allele Identifier: CA393757280

Gene: KIF7

Linked Data

• MyVariant Identifiers: chr15:g.90174862A>T (hg19) ; chr15:g.89631631A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89631631A>T , CM000677.2:g.89631631A>T	GRCh38
NC_000015.9:g.90174862A>T , CM000677.1:g.90174862A>T	GRCh37
NC_000015.8:g.87975866A>T	NCBI36
NG_030338.1:g.28821T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696512.1:c.3098T>A	ENSP00000512678.1:p.Leu1033Gln
ENST00000394412.8:c.2975T>A MANE Select	ENSP00000377934.3:p.Leu992Gln
ENST00000677187.1:n.649T>A
ENST00000394412.7:c.2975T>A	ENSP00000377934.3:p.Leu992Gln
NM_198525.2:c.2975T>A	NP_940927.2:p.Leu992Gln
XM_005254902.2:c.2975T>A	XP_005254959.1:p.Leu992Gln
XM_011521531.1:c.3098T>A	XP_011519833.1:p.Leu1033Gln
XM_011521532.1:c.3095T>A	XP_011519834.1:p.Leu1032Gln
XM_011521533.1:c.3095T>A	XP_011519835.1:p.Leu1032Gln
XM_011521534.1:c.3098T>A	XP_011519836.1:p.Leu1033Gln
XM_011521535.1:c.3098T>A	XP_011519837.1:p.Leu1033Gln
XM_011521536.1:c.3098T>A	XP_011519838.1:p.Leu1033Gln
XM_011521531.2:c.3098T>A	XP_011519833.1:p.Leu1033Gln
NM_198525.3:c.2975T>A MANE Select	NP_940927.2:p.Leu992Gln