Canonical Allele Identifier: CA518222091
Gene: NKAP HGNC NCBI

Linked Data

gnomAD v4: X-119930138-T-C
MyVariant Identifiers: chrX:g.119064101T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119930138T>C , CM000685.2:g.119930138T>C GRCh38
NC_000023.10:g.119064101T>C , CM000685.1:g.119064101T>C GRCh37
NC_000023.9:g.118948129T>C NCBI36
NG_021260.1:g.18635A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371410.5:c.951A>G MANE Select ENSP00000360464.3:p.Glu317=
ENST00000652253.1:c.947A>G
ENST00000371410.4:c.951A>G ENSP00000360464.3:p.Glu317=
ENST00000477789.5:n.1879A>G
ENST00000482407.1:n.750A>G
NM_024528.3:c.951A>G NP_078804.2:p.Glu317=
XM_017029842.1:c.654A>G XP_016885331.1:p.Glu218=
NM_024528.4:c.951A>G MANE Select NP_078804.2:p.Glu317=
Search 100 bp 5'
Search 100 bp 3'