Canonical Allele Identifier: CA338342167

Gene: KIF1B

Linked Data

• ClinVar Variation Id: 2625737
• ClinVar RCV Id: RCV004366453
• MyVariant Identifiers: chr1:g.10403342C>T (hg19) ; chr1:g.10343284C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10343284C>T , CM000663.2:g.10343284C>T	GRCh38
NC_000001.10:g.10403342C>T , CM000663.1:g.10403342C>T	GRCh37
NC_000001.9:g.10325929C>T	NCBI36
NG_008069.1:g.137579C>T , LRG_252:g.137579C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696502.1:c.3547C>T	ENSP00000512668.1:p.Pro1183Ser
ENST00000696503.1:c.3610C>T	ENSP00000512669.1:p.Pro1204Ser
ENST00000696504.1:c.3610C>T	ENSP00000512670.1:p.Pro1204Ser
ENST00000676179.1:c.3685C>T MANE Select	ENSP00000502065.1:p.Pro1229Ser
ENST00000263934.10:c.3547C>T	ENSP00000263934.6:p.Pro1183Ser
ENST00000377081.5:c.3685C>T	ENSP00000366284.1:p.Pro1229Ser
ENST00000377086.5:c.3685C>T	ENSP00000366290.1:p.Pro1229Ser
ENST00000620295.2:c.3643C>T	ENSP00000478500.1:p.Pro1215Ser
ENST00000622724.3:c.3607C>T	ENSP00000480063.1:p.Pro1203Ser
NM_015074.3:c.3547C>T , LRG_252t1:c.3547C>T	NP_055889.2:p.Pro1183Ser
NM_001365951.1:c.3685C>T	NP_001352880.1:p.Pro1229Ser
NM_001365952.1:c.3685C>T	NP_001352881.1:p.Pro1229Ser
NM_001365951.3:c.3685C>T MANE Select	NP_001352880.1:p.Pro1229Ser