Canonical Allele Identifier: CA449458325

Gene: ZFP57

Linked Data

• MyVariant Identifiers: chr6:g.29640421G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672644G>T , CM000668.2:g.29672644G>T	GRCh38
NC_000006.11:g.29640421G>T , CM000668.1:g.29640421G>T	GRCh37
NC_000006.10:g.29748400G>T	NCBI36
NG_013045.1:g.9511C>A
NG_031873.1:g.20664G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376883.2:c.1467C>A MANE Select	ENSP00000366080.2:p.Val489=
ENST00000488757.6:c.1251C>A	ENSP00000418259.2:p.Val417=
ENST00000376881.4:c.1215C>A	ENSP00000366078.4:p.Val405=
ENST00000376883.1:c.1407C>A	ENSP00000366080.1:p.Val469=
ENST00000488757.5:c.1467C>A	ENSP00000418259.1:p.Val489=
NM_001109809.2:c.1467C>A	NP_001103279.2:p.Val489=
XM_006715087.2:c.1251C>A	XP_006715150.1:p.Val417=
XM_011514570.1:c.1467C>A	XP_011512872.1:p.Val489=
NM_001109809.3:c.1467C>A	NP_001103279.2:p.Val489=
NM_001366333.1:c.1251C>A	NP_001353262.1:p.Val417=
NM_001109809.4:c.1467C>A	NP_001103279.2:p.Val489=
NM_001366333.2:c.1251C>A	NP_001353262.1:p.Val417=
NM_001109809.5:c.1467C>A MANE Select	NP_001103279.2:p.Val489=