Canonical Allele Identifier: CA415883389

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10397478T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10337420T>C , CM000663.2:g.10337420T>C	GRCh38
NC_000001.10:g.10397478T>C , CM000663.1:g.10397478T>C	GRCh37
NC_000001.9:g.10320065T>C	NCBI36
NG_008069.1:g.131715T>C , LRG_252:g.131715T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.3171T>C	ENSP00000512668.1:p.Phe1057=
ENST00000696503.1:c.3234T>C	ENSP00000512669.1:p.Phe1078=
ENST00000696504.1:c.3234T>C	ENSP00000512670.1:p.Phe1078=
ENST00000676179.1:c.3309T>C MANE Select	ENSP00000502065.1:p.Phe1103=
ENST00000263934.10:c.3171T>C	ENSP00000263934.6:p.Phe1057=
ENST00000377081.5:c.3309T>C	ENSP00000366284.1:p.Phe1103=
ENST00000377086.5:c.3309T>C	ENSP00000366290.1:p.Phe1103=
ENST00000620295.2:c.3267T>C	ENSP00000478500.1:p.Phe1089=
ENST00000622724.3:c.3231T>C	ENSP00000480063.1:p.Phe1077=
NM_015074.3:c.3171T>C , LRG_252t1:c.3171T>C	NP_055889.2:p.Phe1057=
NM_001365951.1:c.3309T>C	NP_001352880.1:p.Phe1103=
NM_001365952.1:c.3309T>C	NP_001352881.1:p.Phe1103=
NM_001365951.3:c.3309T>C MANE Select	NP_001352880.1:p.Phe1103=