Canonical Allele Identifier: CA414771509
Gene: ZIC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.136651129A>C (hg19) chrX:g.137568970A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.137568970A>C , CM000685.2:g.137568970A>C GRCh38
NC_000023.10:g.136651129A>C , CM000685.1:g.136651129A>C GRCh37
NC_000023.9:g.136478795A>C NCBI36
NG_008115.1:g.7784A>C
NG_008115.2:g.7844A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287538.10:c.1129A>C MANE Select ENSP00000287538.5:p.Lys377Gln
ENST00000287538.9:c.1129A>C ENSP00000287538.5:p.Lys377Gln
ENST00000370606.3:c.1129A>C ENSP00000359638.3:p.Lys377Gln
ENST00000478471.1:n.166A>C
NM_003413.3:c.1129A>C NP_003404.1:p.Lys377Gln
NM_001330661.1:c.1129A>C NP_001317590.1:p.Lys377Gln
NM_003413.4:c.1129A>C MANE Select NP_003404.1:p.Lys377Gln
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