Canonical Allele Identifier: CA338343578

Gene: KIF1B

Linked Data

• MyVariant Identifiers: chr1:g.10408732C>G (hg19) ; chr1:g.10348674C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10348674C>G , CM000663.2:g.10348674C>G	GRCh38
NC_000001.10:g.10408732C>G , CM000663.1:g.10408732C>G	GRCh37
NC_000001.9:g.10331319C>G	NCBI36
NG_008069.1:g.142969C>G , LRG_252:g.142969C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3953C>G	ENSP00000512668.1:p.Thr1318Ser
ENST00000696503.1:c.3815C>G	ENSP00000512669.1:p.Thr1272Ser
ENST00000696504.1:c.3815C>G	ENSP00000512670.1:p.Thr1272Ser
ENST00000676179.1:c.3890C>G MANE Select	ENSP00000502065.1:p.Thr1297Ser
ENST00000263934.10:c.3752C>G	ENSP00000263934.6:p.Thr1251Ser
ENST00000377081.5:c.3890C>G	ENSP00000366284.1:p.Thr1297Ser
ENST00000377086.5:c.3890C>G	ENSP00000366290.1:p.Thr1297Ser
ENST00000465635.5:n.345C>G
ENST00000483340.1:n.426C>G
ENST00000620295.2:c.3848C>G	ENSP00000478500.1:p.Thr1283Ser
ENST00000622724.3:c.3812C>G	ENSP00000480063.1:p.Thr1271Ser
NM_015074.3:c.3752C>G , LRG_252t1:c.3752C>G	NP_055889.2:p.Thr1251Ser
NM_001365951.1:c.3890C>G	NP_001352880.1:p.Thr1297Ser
NM_001365952.1:c.3890C>G	NP_001352881.1:p.Thr1297Ser
NM_001365951.3:c.3890C>G MANE Select	NP_001352880.1:p.Thr1297Ser