Canonical Allele Identifier: CA449458327
Gene: ZFP57 HGNC NCBI

Linked Data

gnomAD v4: 6-29672647-A-G
MyVariant Identifiers: chr6:g.29640424A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29672647A>G , CM000668.2:g.29672647A>G GRCh38
NC_000006.11:g.29640424A>G , CM000668.1:g.29640424A>G GRCh37
NC_000006.10:g.29748403A>G NCBI36
NG_013045.1:g.9508T>C
NG_031873.1:g.20667A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376883.2:c.1464T>C MANE Select ENSP00000366080.2:p.Asp488=
ENST00000488757.6:c.1248T>C ENSP00000418259.2:p.Asp416=
ENST00000376881.4:c.1212T>C ENSP00000366078.4:p.Asp404=
ENST00000376883.1:c.1404T>C ENSP00000366080.1:p.Asp468=
ENST00000488757.5:c.1464T>C ENSP00000418259.1:p.Asp488=
NM_001109809.2:c.1464T>C NP_001103279.2:p.Asp488=
XM_006715087.2:c.1248T>C XP_006715150.1:p.Asp416=
XM_011514570.1:c.1464T>C XP_011512872.1:p.Asp488=
NM_001109809.3:c.1464T>C NP_001103279.2:p.Asp488=
NM_001366333.1:c.1248T>C NP_001353262.1:p.Asp416=
NM_001109809.4:c.1464T>C NP_001103279.2:p.Asp488=
NM_001366333.2:c.1248T>C NP_001353262.1:p.Asp416=
NM_001109809.5:c.1464T>C MANE Select NP_001103279.2:p.Asp488=