Canonical Allele Identifier: CA363043409
Gene: ZFP57 HGNC NCBI

Linked Data

gnomAD v4: 6-29672763-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29672763C>A , CM000668.2:g.29672763C>A GRCh38
NC_000006.11:g.29640540C>A , CM000668.1:g.29640540C>A GRCh37
NC_000006.10:g.29748519C>A NCBI36
NG_013045.1:g.9392G>T
NG_031873.1:g.20783C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376883.2:c.1348G>T MANE Select ENSP00000366080.2:p.Gly450Trp
ENST00000488757.6:c.1132G>T ENSP00000418259.2:p.Gly378Trp
ENST00000376881.4:c.1096G>T ENSP00000366078.4:p.Gly366Trp
ENST00000376883.1:c.1288G>T ENSP00000366080.1:p.Gly430Trp
ENST00000488757.5:c.1348G>T ENSP00000418259.1:p.Gly450Trp
NM_001109809.2:c.1348G>T NP_001103279.2:p.Gly450Trp
XM_006715087.2:c.1132G>T XP_006715150.1:p.Gly378Trp
XM_011514570.1:c.1348G>T XP_011512872.1:p.Gly450Trp
NM_001109809.3:c.1348G>T NP_001103279.2:p.Gly450Trp
NM_001366333.1:c.1132G>T NP_001353262.1:p.Gly378Trp
NM_001109809.4:c.1348G>T NP_001103279.2:p.Gly450Trp
NM_001366333.2:c.1132G>T NP_001353262.1:p.Gly378Trp
NM_001109809.5:c.1348G>T MANE Select NP_001103279.2:p.Gly450Trp