Canonical Allele Identifier: CA415883434

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10397490T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10337432T>A , CM000663.2:g.10337432T>A	GRCh38
NC_000001.10:g.10397490T>A , CM000663.1:g.10397490T>A	GRCh37
NC_000001.9:g.10320077T>A	NCBI36
NG_008069.1:g.131727T>A , LRG_252:g.131727T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.3183T>A	ENSP00000512668.1:p.Ile1061=
ENST00000696503.1:c.3246T>A	ENSP00000512669.1:p.Ile1082=
ENST00000696504.1:c.3246T>A	ENSP00000512670.1:p.Ile1082=
ENST00000676179.1:c.3321T>A MANE Select	ENSP00000502065.1:p.Ile1107=
ENST00000263934.10:c.3183T>A	ENSP00000263934.6:p.Ile1061=
ENST00000377081.5:c.3321T>A	ENSP00000366284.1:p.Ile1107=
ENST00000377086.5:c.3321T>A	ENSP00000366290.1:p.Ile1107=
ENST00000620295.2:c.3279T>A	ENSP00000478500.1:p.Ile1093=
ENST00000622724.3:c.3243T>A	ENSP00000480063.1:p.Ile1081=
NM_015074.3:c.3183T>A , LRG_252t1:c.3183T>A	NP_055889.2:p.Ile1061=
NM_001365951.1:c.3321T>A	NP_001352880.1:p.Ile1107=
NM_001365952.1:c.3321T>A	NP_001352881.1:p.Ile1107=
NM_001365951.3:c.3321T>A MANE Select	NP_001352880.1:p.Ile1107=