Canonical Allele Identifier: CA407255053
Community Standard Title: NM_017652.4(ZNF586):c.10G>T (p.Ala4Ser)
Gene: ZNF586 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57769852G>T , CM000681.2:g.57769852G>T GRCh38
NC_000019.9:g.58281220G>T , CM000681.1:g.58281220G>T GRCh37
NC_000019.8:g.62973032G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_017652.4:c.10G>T MANE Select NP_060122.2:p.Ala4Ser
ENST00000396154.7:c.10G>T MANE Select ENSP00000379458.1:p.Ala4Ser
NM_001077426.2:c.10G>T NP_001070894.1:p.Ala4Ser
NM_001077426.3:c.10G>T NP_001070894.1:p.Ala4Ser
NM_001204814.1:c.-170G>T NP_001191743.1:n.-170G>T
NM_001204814.2:c.-170G>T NP_001191743.1:n.-170G>T
NM_017652.3:c.10G>T NP_060122.2:p.Ala4Ser
ENST00000391702.3:c.-170G>T ENSP00000375583.3:n.-170G>T
ENST00000396150.4:c.10G>T ENSP00000379454.3:p.Ala4Ser
ENST00000396154.6:c.10G>T ENSP00000379458.1:p.Ala4Ser
ENST00000598183.1:c.10G>T ENSP00000471663.1:p.Ala4Ser
ENST00000598885.5:c.10G>T ENSP00000470397.1:p.Ala4Ser
ENST00000599802.1:c.10G>T ENSP00000472972.1:p.Ala4Ser
ENST00000651718.1:c.10G>T ENSP00000498256.1:p.Ala4Ser