Canonical Allele Identifier: CA581874

Gene: KIF1B

Linked Data

• dbSNP Id: rs755338239
• ExAC: 1:10406049 T / TCTG
• MyVariant Identifiers: chr1:g.10406049_10406050insCTG (hg19) ; chr1:g.10345991_10345992insCTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10345991_10345992insCTG , CM000663.2:g.10345991_10345992insCTG	GRCh38
NC_000001.10:g.10406049_10406050insCTG , CM000663.1:g.10406049_10406050insCTG	GRCh37
NC_000001.9:g.10328636_10328637insCTG	NCBI36
NG_008069.1:g.140286_140287insCTG , LRG_252:g.140286_140287insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3860+38_3860+39insCTG	ENSP00000512668.1:n.3860+38_3860+39insCTG
ENST00000696503.1:c.3722+38_3722+39insCTG	ENSP00000512669.1:n.3722+38_3722+39insCTG
ENST00000696504.1:c.3722+38_3722+39insCTG	ENSP00000512670.1:n.3722+38_3722+39insCTG
ENST00000676179.1:c.3797+38_3797+39insCTG MANE Select	ENSP00000502065.1:n.3797+38_3797+39insCTG
ENST00000263934.10:c.3659+38_3659+39insCTG	ENSP00000263934.6:n.3659+38_3659+39insCTG
ENST00000377081.5:c.3797+38_3797+39insCTG	ENSP00000366284.1:n.3797+38_3797+39insCTG
ENST00000377086.5:c.3797+38_3797+39insCTG	ENSP00000366290.1:n.3797+38_3797+39insCTG
ENST00000465635.5:n.252+38_252+39insCTG
ENST00000483340.1:n.333+38_333+39insCTG
ENST00000620295.2:c.3755+38_3755+39insCTG	ENSP00000478500.1:n.3755+38_3755+39insCTG
ENST00000622724.3:c.3719+38_3719+39insCTG	ENSP00000480063.1:n.3719+38_3719+39insCTG
NM_015074.3:c.3659+38_3659+39insCTG , LRG_252t1:c.3659+38_3659+39insCTG	NP_055889.2:n.3659+38_3659+39insCTG
NM_001365951.1:c.3797+38_3797+39insCTG	NP_001352880.1:n.3797+38_3797+39insCTG
NM_001365952.1:c.3797+38_3797+39insCTG	NP_001352881.1:n.3797+38_3797+39insCTG
NM_001365951.3:c.3797+38_3797+39insCTG MANE Select	NP_001352880.1:n.3797+38_3797+39insCTG