Canonical Allele Identifier: CA415881413
Gene: KIF1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.10380154G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.10320096G>T , CM000663.2:g.10320096G>T GRCh38
NC_000001.10:g.10380154G>T , CM000663.1:g.10380154G>T GRCh37
NC_000001.9:g.10302741G>T NCBI36
NG_008069.1:g.114391G>T , LRG_252:g.114391G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696502.1:c.2031G>T ENSP00000512668.1:p.Leu677=
ENST00000696503.1:c.2094G>T ENSP00000512669.1:p.Leu698=
ENST00000696504.1:c.2094G>T ENSP00000512670.1:p.Leu698=
ENST00000676179.1:c.2169G>T MANE Select ENSP00000502065.1:p.Leu723=
ENST00000263934.10:c.2031G>T ENSP00000263934.6:p.Leu677=
ENST00000377081.5:c.2169G>T ENSP00000366284.1:p.Leu723=
ENST00000377086.5:c.2169G>T ENSP00000366290.1:p.Leu723=
ENST00000620295.2:c.2127G>T ENSP00000478500.1:p.Leu709=
ENST00000622724.3:c.2091G>T ENSP00000480063.1:p.Leu697=
NM_015074.3:c.2031G>T , LRG_252t1:c.2031G>T NP_055889.2:p.Leu677=
NM_001365951.1:c.2169G>T NP_001352880.1:p.Leu723=
NM_001365952.1:c.2169G>T NP_001352881.1:p.Leu723=
NM_001365951.3:c.2169G>T MANE Select NP_001352880.1:p.Leu723=