Canonical Allele Identifier: CA497555131

Linked Data

gnomAD v4: 17-5002466-G-C
MyVariant Identifiers: chr17:g.4905761G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.5002466G>C , CM000679.2:g.5002466G>C GRCh38
NC_000017.10:g.4905761G>C , CM000679.1:g.4905761G>C GRCh37
NC_000017.9:g.4846485G>C NCBI36
NG_034137.1:g.9519G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320785.10:c.432G>C (KIF1C) MANE Select ENSP00000320821.5:p.Val144=
ENST00000320785.9:c.432G>C (KIF1C) ENSP00000320821.5:p.Val144=
NM_006612.5:c.432G>C (KIF1C) NP_006603.2:p.Val144=
XM_005256424.1:c.432G>C (KIF1C) XP_005256481.1:p.Val144=
XM_005256424.2:c.432G>C (KIF1C) XP_005256481.1:p.Val144=
XM_024450745.1:c.-39+3616C>G (INCA1) XP_024306513.1:n.-39+3616C>G
NM_006612.6:c.432G>C (KIF1C) MANE Select NP_006603.2:p.Val144=