Canonical Allele Identifier: CA15362953

Gene: KIF3A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132713335C>T , CM000667.2:g.132713335C>T	GRCh38
NC_000005.9:g.132049027C>T , CM000667.1:g.132049027C>T	GRCh37
NC_000005.8:g.132076926C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403231.6:c.1130-2278G>A MANE Select	ENSP00000385808.1:n.1130-2278G>A
ENST00000378735.5:c.1130-2278G>A	ENSP00000368009.1:n.1130-2278G>A
ENST00000378746.8:c.1130-2278G>A	ENSP00000368020.3:n.1130-2278G>A
ENST00000403231.5:c.1130-2278G>A	ENSP00000385808.1:n.1130-2278G>A
ENST00000618515.4:c.1130-2281G>A	ENSP00000483023.1:n.1130-2281G>A
NM_001300791.1:c.1130-2278G>A	NP_001287720.1:n.1130-2278G>A
NM_001300792.1:c.1130-2278G>A	NP_001287721.1:n.1130-2278G>A
NM_007054.6:c.1130-2278G>A	NP_008985.3:n.1130-2278G>A
XM_006714526.2:c.1130-2278G>A	XP_006714589.1:n.1130-2278G>A
XM_006714526.4:c.1130-2278G>A	XP_006714589.1:n.1130-2278G>A
XM_017008995.2:c.1130-2278G>A	XP_016864484.1:n.1130-2278G>A
XM_017008996.2:c.1130-2278G>A	XP_016864485.1:n.1130-2278G>A
NM_001300791.2:c.1130-2278G>A MANE Select	NP_001287720.1:n.1130-2278G>A
NM_001300792.2:c.1130-2278G>A	NP_001287721.1:n.1130-2278G>A
NM_007054.7:c.1130-2278G>A	NP_008985.3:n.1130-2278G>A