Canonical Allele Identifier: CA8219865
Gene: ZCCHC14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87412371C>T , CM000678.2:g.87412371C>T GRCh38
NC_000016.9:g.87445977C>T , CM000678.1:g.87445977C>T GRCh37
NC_000016.8:g.86003478C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_015144.3:c.2350G>A MANE Select NP_055959.2:p.Ala784Thr
ENST00000671377.2:c.2350G>A MANE Select ENSP00000499622.1:p.Ala784Thr
NM_015144.2:c.1939G>A NP_055959.1:p.Ala647Thr
ENST00000268616.8:c.1939G>A ENSP00000268616.4:p.Ala647Thr
ENST00000268616.9:c.1939G>A ENSP00000268616.4:p.Ala647Thr
ENST00000561928.1:c.1589G>A
ENST00000568020.5:c.1939G>A ENSP00000455431.1:p.Ala647Thr
ENST00000568020.6:c.1971G>A
XM_005255858.3:c.1939G>A XP_005255915.2:p.Ala647Thr
XM_017023082.2:c.1831G>A XP_016878571.1:p.Ala611Thr
XR_243401.3:n.2157G>A