Canonical Allele Identifier: CA2643184534

Gene: KIF1B

Linked Data

• gnomAD v4: 1-10365387-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10365387G>T , CM000663.2:g.10365387G>T	GRCh38
NC_000001.10:g.10425445G>T , CM000663.1:g.10425445G>T	GRCh37
NC_000001.9:g.10348032G>T	NCBI36
NG_008069.1:g.159682G>T , LRG_252:g.159682G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.4576-22G>T	ENSP00000512668.1:n.4576-22G>T
ENST00000696503.1:c.4438-22G>T	ENSP00000512669.1:n.4438-22G>T
ENST00000696504.1:c.4438-22G>T	ENSP00000512670.1:n.4438-22G>T
ENST00000676179.1:c.4513-22G>T MANE Select	ENSP00000502065.1:n.4513-22G>T
ENST00000263934.10:c.4375-22G>T	ENSP00000263934.6:n.4375-22G>T
ENST00000377081.5:c.4513-22G>T	ENSP00000366284.1:n.4513-22G>T
ENST00000377086.5:c.4513-22G>T	ENSP00000366290.1:n.4513-22G>T
ENST00000470616.1:n.222G>T
ENST00000620295.2:c.4471-22G>T	ENSP00000478500.1:n.4471-22G>T
ENST00000622724.3:c.4435-22G>T	ENSP00000480063.1:n.4435-22G>T
ENST00000635499.1:c.558-22G>T
NM_015074.3:c.4375-22G>T , LRG_252t1:c.4375-22G>T	NP_055889.2:n.4375-22G>T
XR_946953.1:n.355+994C>A
NM_001365951.1:c.4513-22G>T	NP_001352880.1:n.4513-22G>T
NM_001365952.1:c.4513-22G>T	NP_001352881.1:n.4513-22G>T
XR_946953.2:n.230+994C>A
NM_001365951.3:c.4513-22G>T MANE Select	NP_001352880.1:n.4513-22G>T