Canonical Allele Identifier: CA930309081
Gene: ZCCHC24 HGNC NCBI

Linked Data

dbSNP Id: rs1857016241

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79425609del , CM000672.2:g.79425609del GRCh38
NC_000010.10:g.81185365del , CM000672.1:g.81185365del GRCh37
NC_000010.9:g.80855371del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372336.4:c.447+6949del MANE Select ENSP00000361411.3:n.447+6949del
ENST00000372333.3:c.268+6949del ENSP00000361408.3:n.268+6949del
ENST00000372336.3:c.447+6949del ENSP00000361411.3:n.447+6949del
NM_153367.3:c.447+6949del NP_699198.2:n.447+6949del
XM_011539452.1:c.237+6949del XP_011537754.1:n.237+6949del
XM_011539452.3:c.237+6949del XP_011537754.1:n.237+6949del
NM_153367.4:c.447+6949del MANE Select NP_699198.2:n.447+6949del