Canonical Allele Identifier: CA363043362

Gene: ZFP57

Linked Data

• MyVariant Identifiers: chr6:g.29640520C>A (hg19) ; chr6:g.29672743C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672743C>A , CM000668.2:g.29672743C>A	GRCh38
NC_000006.11:g.29640520C>A , CM000668.1:g.29640520C>A	GRCh37
NC_000006.10:g.29748499C>A	NCBI36
NG_013045.1:g.9412G>T
NG_031873.1:g.20763C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376883.2:c.1368G>T MANE Select	ENSP00000366080.2:p.Met456Ile
ENST00000488757.6:c.1152G>T	ENSP00000418259.2:p.Met384Ile
ENST00000376881.4:c.1116G>T	ENSP00000366078.4:p.Met372Ile
ENST00000376883.1:c.1308G>T	ENSP00000366080.1:p.Met436Ile
ENST00000488757.5:c.1368G>T	ENSP00000418259.1:p.Met456Ile
NM_001109809.2:c.1368G>T	NP_001103279.2:p.Met456Ile
XM_006715087.2:c.1152G>T	XP_006715150.1:p.Met384Ile
XM_011514570.1:c.1368G>T	XP_011512872.1:p.Met456Ile
NM_001109809.3:c.1368G>T	NP_001103279.2:p.Met456Ile
NM_001366333.1:c.1152G>T	NP_001353262.1:p.Met384Ile
NM_001109809.4:c.1368G>T	NP_001103279.2:p.Met456Ile
NM_001366333.2:c.1152G>T	NP_001353262.1:p.Met384Ile
NM_001109809.5:c.1368G>T MANE Select	NP_001103279.2:p.Met456Ile