Canonical Allele Identifier: CA2240462911

Gene: ZCCHC14

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87428363G>C , CM000678.2:g.87428363G>C	GRCh38
NC_000016.9:g.87461969G>C , CM000678.1:g.87461969G>C	GRCh37
NC_000016.8:g.86019470G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268616.9:c.358-4482C>G	ENSP00000268616.4:n.358-4482C>G
ENST00000568020.6:c.390-4482C>G
ENST00000671377.2:c.769-4482C>G MANE Select	ENSP00000499622.1:n.769-4482C>G
ENST00000268616.8:c.358-4482C>G	ENSP00000268616.4:n.358-4482C>G
ENST00000561928.1:c.8-4482C>G
ENST00000568020.5:c.358-4482C>G	ENSP00000455431.1:n.358-4482C>G
NM_015144.2:c.358-4482C>G	NP_055959.1:n.358-4482C>G
XM_005255858.3:c.358-4482C>G	XP_005255915.2:n.358-4482C>G
XM_011522963.1:c.769-4482C>G	XP_011521265.1:n.769-4482C>G
XM_011522964.1:c.769-4482C>G	XP_011521266.1:n.769-4482C>G
XR_243401.3:n.576-4482C>G
XM_011522964.2:c.769-4482C>G	XP_011521266.1:n.769-4482C>G
XM_017023082.2:c.250-4482C>G	XP_016878571.1:n.250-4482C>G
NM_015144.3:c.769-4482C>G MANE Select	NP_055959.2:n.769-4482C>G