Canonical Allele Identifier: CA497555208

Linked Data

MyVariant Identifiers: chr17:g.4905834C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002539C>A , CM000679.2:g.5002539C>A GRCh38
NC_000017.10:g.4905834C>A , CM000679.1:g.4905834C>A GRCh37
NC_000017.9:g.4846558C>A NCBI36
NG_034137.1:g.9592C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320785.10:c.505C>A (KIF1C) MANE Select ENSP00000320821.5:p.Arg169=
ENST00000320785.9:c.505C>A (KIF1C) ENSP00000320821.5:p.Arg169=
NM_006612.5:c.505C>A (KIF1C) NP_006603.2:p.Arg169=
XM_005256424.1:c.505C>A (KIF1C) XP_005256481.1:p.Arg169=
XM_005256424.2:c.505C>A (KIF1C) XP_005256481.1:p.Arg169=
XM_024450745.1:c.-39+3543G>T (INCA1) XP_024306513.1:n.-39+3543G>T
NM_006612.6:c.505C>A (KIF1C) MANE Select NP_006603.2:p.Arg169=