Canonical Allele Identifier: CA449458244
Gene: ZFP57 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.29640439A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29672662A>T , CM000668.2:g.29672662A>T GRCh38
NC_000006.11:g.29640439A>T , CM000668.1:g.29640439A>T GRCh37
NC_000006.10:g.29748418A>T NCBI36
NG_013045.1:g.9493T>A
NG_031873.1:g.20682A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376883.2:c.1449T>A MANE Select ENSP00000366080.2:p.Leu483=
ENST00000488757.6:c.1233T>A ENSP00000418259.2:p.Leu411=
ENST00000376881.4:c.1197T>A ENSP00000366078.4:p.Leu399=
ENST00000376883.1:c.1389T>A ENSP00000366080.1:p.Leu463=
ENST00000488757.5:c.1449T>A ENSP00000418259.1:p.Leu483=
NM_001109809.2:c.1449T>A NP_001103279.2:p.Leu483=
XM_006715087.2:c.1233T>A XP_006715150.1:p.Leu411=
XM_011514570.1:c.1449T>A XP_011512872.1:p.Leu483=
NM_001109809.3:c.1449T>A NP_001103279.2:p.Leu483=
NM_001366333.1:c.1233T>A NP_001353262.1:p.Leu411=
NM_001109809.4:c.1449T>A NP_001103279.2:p.Leu483=
NM_001366333.2:c.1233T>A NP_001353262.1:p.Leu411=
NM_001109809.5:c.1449T>A MANE Select NP_001103279.2:p.Leu483=