Canonical Allele Identifier: CA690170962
Gene: ZC3H10 HGNC NCBI
ESYT1 HGNC NCBI

Linked Data

dbSNP Id: rs1490921917
MyVariant Identifiers: chr12:g.56518358_56518363del (hg19) chr12:g.56124574_56124579del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56124578_56124583del , CM000674.2:g.56124578_56124583del GRCh38
NC_000012.11:g.56518362_56518367del , CM000674.1:g.56518362_56518367del GRCh37
NC_000012.10:g.54804629_54804634del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000257940.7:c.*2711_*2716del (ZC3H10) MANE Select ENSP00000257940.2:n.*2711_*2716del
ENST00000257940.6:c.*2711_*2716del (ZC3H10) ENSP00000257940.2:n.*2711_*2716del
ENST00000551790.5:c.-143-3962_-143-3957del (ESYT1) ENSP00000447756.1:n.-143-3962_-143-3957del
NM_032786.3:c.*2711_*2716del (ZC3H10) MANE Select NP_116175.1:n.*2711_*2716del
NM_001303124.2:c.*2711_*2716del (ZC3H10) NP_001290053.1:n.*2711_*2716del
NM_001303125.2:c.*2711_*2716del (ZC3H10) NP_001290054.1:n.*2711_*2716del
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