Canonical Allele Identifier: CA2454712027
Gene: NKAP HGNC NCBI

Linked Data

dbSNP Id: rs2056733490

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930196C>G , CM000685.2:g.119930196C>G GRCh38
NC_000023.10:g.119064159C>G , CM000685.1:g.119064159C>G GRCh37
NC_000023.9:g.118948187C>G NCBI36
NG_021260.1:g.18577G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371410.5:c.924-31G>C MANE Select ENSP00000360464.3:n.924-31G>C
ENST00000652253.1:c.920-31G>C
ENST00000371410.4:c.924-31G>C ENSP00000360464.3:n.924-31G>C
ENST00000477789.5:n.1852-31G>C
ENST00000482407.1:n.723-31G>C
NM_024528.3:c.924-31G>C NP_078804.2:n.924-31G>C
XM_017029842.1:c.627-31G>C XP_016885331.1:n.627-31G>C
NM_024528.4:c.924-31G>C MANE Select NP_078804.2:n.924-31G>C