Canonical Allele Identifier: CA10636646

Gene: KIF7 TICRR

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89627997dup , CM000677.2:g.89627997dup	GRCh38
NC_000015.9:g.90171228dup , CM000677.1:g.90171228dup	GRCh37
NC_000015.8:g.87972232dup	NCBI36
NG_030338.1:g.32463dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.*430dup (KIF7)	ENSP00000512678.1:n.*430dup
ENST00000268138.12:c.*911dup (TICRR) MANE Select	ENSP00000268138.7:n.*911dup
ENST00000394412.8:c.*430dup (KIF7) MANE Select	ENSP00000377934.3:n.*430dup
ENST00000268138.11:c.*911dup (TICRR)	ENSP00000268138.7:n.*911dup
ENST00000394412.7:c.*430dup (KIF7)	ENSP00000377934.3:n.*430dup
ENST00000558928.1:n.180+612dup (KIF7)
ENST00000560985.5:c.6641dup (TICRR)	ENSP00000453306.1:n.6641dup
ENST00000561095.1:c.740+815dup (TICRR)
NM_001308025.1:c.6641dup (TICRR)	NP_001294954.1:n.6641dup
NM_152259.3:c.6644dup (TICRR)	NP_689472.3:n.6644dup
NM_198525.2:c.*430dup (KIF7)	NP_940927.2:n.*430dup
XM_005254902.2:c.*430dup (KIF7)	XP_005254959.1:n.*430dup
XM_011521531.1:c.*430dup (KIF7)	XP_011519833.1:n.*430dup
XM_011521532.1:c.*430dup (KIF7)	XP_011519834.1:n.*430dup
XM_011521533.1:c.*430dup (KIF7)	XP_011519835.1:n.*430dup
XM_011521534.1:c.3973+612dup (KIF7)	XP_011519836.1:n.3973+612dup
XM_011521535.1:c.3973+612dup (KIF7)	XP_011519837.1:n.3973+612dup
XM_011521536.1:c.3973+612dup (KIF7)	XP_011519838.1:n.3973+612dup
XM_011522162.1:c.*911dup (TICRR)	XP_011520464.1:n.*911dup
XM_011521531.2:c.*430dup (KIF7)	XP_011519833.1:n.*430dup
NM_198525.3:c.*430dup (KIF7) MANE Select	NP_940927.2:n.*430dup
NM_152259.4:c.*911dup (TICRR) MANE Select	NP_689472.3:n.*911dup