Canonical Allele Identifier: CA415884319

Gene: KIF1B

Linked Data

• gnomAD v4: 1-10343235-G-T
• MyVariant Identifiers: chr1:g.10403293G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10343235G>T , CM000663.2:g.10343235G>T	GRCh38
NC_000001.10:g.10403293G>T , CM000663.1:g.10403293G>T	GRCh37
NC_000001.9:g.10325880G>T	NCBI36
NG_008069.1:g.137530G>T , LRG_252:g.137530G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696502.1:c.3498G>T	ENSP00000512668.1:p.Pro1166=
ENST00000696503.1:c.3561G>T	ENSP00000512669.1:p.Pro1187=
ENST00000696504.1:c.3561G>T	ENSP00000512670.1:p.Pro1187=
ENST00000676179.1:c.3636G>T MANE Select	ENSP00000502065.1:p.Pro1212=
ENST00000263934.10:c.3498G>T	ENSP00000263934.6:p.Pro1166=
ENST00000377081.5:c.3636G>T	ENSP00000366284.1:p.Pro1212=
ENST00000377086.5:c.3636G>T	ENSP00000366290.1:p.Pro1212=
ENST00000620295.2:c.3594G>T	ENSP00000478500.1:p.Pro1198=
ENST00000622724.3:c.3558G>T	ENSP00000480063.1:p.Pro1186=
NM_015074.3:c.3498G>T , LRG_252t1:c.3498G>T	NP_055889.2:p.Pro1166=
NM_001365951.1:c.3636G>T	NP_001352880.1:p.Pro1212=
NM_001365952.1:c.3636G>T	NP_001352881.1:p.Pro1212=
NM_001365951.3:c.3636G>T MANE Select	NP_001352880.1:p.Pro1212=