Canonical Allele Identifier: CA1922181195
Gene: ZCCHC24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79425608_79425609delinsAC , CM000672.2:g.79425608_79425609delinsAC GRCh38
NC_000010.10:g.81185364_81185365delinsAC , CM000672.1:g.81185364_81185365delinsAC GRCh37
NC_000010.9:g.80855370_80855371delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372336.4:c.447+6949_447+6950delinsGT MANE Select ENSP00000361411.3:n.447+6949_447+6950delinsGT
ENST00000372333.3:c.268+6949_268+6950delinsGT ENSP00000361408.3:n.268+6949_268+6950delinsGT
ENST00000372336.3:c.447+6949_447+6950delinsGT ENSP00000361411.3:n.447+6949_447+6950delinsGT
NM_153367.3:c.447+6949_447+6950delinsGT NP_699198.2:n.447+6949_447+6950delinsGT
XM_011539452.1:c.237+6949_237+6950delinsGT XP_011537754.1:n.237+6949_237+6950delinsGT
XM_011539452.3:c.237+6949_237+6950delinsGT XP_011537754.1:n.237+6949_237+6950delinsGT
NM_153367.4:c.447+6949_447+6950delinsGT MANE Select NP_699198.2:n.447+6949_447+6950delinsGT