Canonical Allele Identifier: CA1613369466

Gene: KIF13A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.17813594C= , CM000668.2:g.17813594C=	GRCh38
NC_000006.11:g.17813825C= , CM000668.1:g.17813825C=	GRCh37
NC_000006.10:g.17921804C=	NCBI36
NG_029766.1:g.179030G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259711.11:c.2000+3426G= MANE Select	ENSP00000259711.6:n.2000+3426G=
ENST00000636847.1:c.2120+3426G=	ENSP00000490031.1:n.2120+3426G=
ENST00000259711.10:c.2000+3426G=	ENSP00000259711.6:n.2000+3426G=
ENST00000358380.10:c.181+3426G=
ENST00000378814.9:c.2000+3426G=	ENSP00000368091.5:n.2000+3426G=
ENST00000378826.6:c.2000+3426G=	ENSP00000368103.2:n.2000+3426G=
ENST00000378843.6:c.2000+3426G=	ENSP00000368120.2:n.2000+3426G=
ENST00000503342.1:n.172-984G=
NM_001105566.2:c.2000+3426G=	NP_001099036.1:n.2000+3426G=
NM_001105567.2:c.2000+3426G=	NP_001099037.1:n.2000+3426G=
NM_001105568.2:c.2000+3426G=	NP_001099038.1:n.2000+3426G=
NM_022113.5:c.2000+3426G=	NP_071396.4:n.2000+3426G=
XM_005249289.1:c.2120+3426G=	XP_005249346.1:n.2120+3426G=
XM_005249290.1:c.2120+3426G=	XP_005249347.1:n.2120+3426G=
XM_005249291.1:c.2120+3426G=	XP_005249348.1:n.2120+3426G=
XM_005249292.1:c.2120+3426G=	XP_005249349.1:n.2120+3426G=
XM_005249293.1:c.2120+3426G=	XP_005249350.1:n.2120+3426G=
XM_006715166.1:c.1931+3426G=	XP_006715229.1:n.1931+3426G=
XM_011514805.1:c.1787+3426G=	XP_011513107.1:n.1787+3426G=
XM_017011188.1:c.2000+3426G=	XP_016866677.1:n.2000+3426G=
XM_017011189.1:c.2000+3426G=	XP_016866678.1:n.2000+3426G=
XM_017011190.1:c.2000+3426G=	XP_016866679.1:n.2000+3426G=
XM_017011192.1:c.2000+3426G=	XP_016866681.1:n.2000+3426G=
XM_017011193.1:c.1667+3426G=	XP_016866682.1:n.1667+3426G=
NM_022113.6:c.2000+3426G= MANE Select	NP_071396.4:n.2000+3426G=
NM_001105566.3:c.2000+3426G=	NP_001099036.1:n.2000+3426G=
NM_001105567.3:c.2000+3426G=	NP_001099037.1:n.2000+3426G=
NM_001105568.3:c.2000+3426G=	NP_001099038.1:n.2000+3426G=
NM_001105568.4:c.2000+3426G=	NP_001099038.1:n.2000+3426G=