Canonical Allele Identifier: CA8014945

Gene: ZNF629 RNF40

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30782664C>G , CM000678.2:g.30782664C>G	GRCh38
NC_000016.9:g.30793985C>G , CM000678.1:g.30793985C>G	GRCh37
NC_000016.8:g.30701486C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001080417.3:c.1664G>C (ZNF629) MANE Select	NP_001073886.1:p.Gly555Ala
ENST00000262525.6:c.1664G>C (ZNF629) MANE Select	ENSP00000262525.4:p.Gly555Ala
NM_001080417.1:c.1664G>C (ZNF629)	NP_001073886.1:p.Gly555Ala
NM_001080417.2:c.1664G>C (ZNF629)	NP_001073886.1:p.Gly555Ala
NM_001345970.1:c.1622G>C (ZNF629)	NP_001332899.1:p.Gly541Ala
NM_001345970.2:c.1622G>C (ZNF629)	NP_001332899.1:p.Gly541Ala
ENST00000262525.5:c.1664G>C (ZNF629)	ENSP00000262525.4:p.Gly555Ala
XM_005255222.2:c.1622G>C (ZNF629)	XP_005255279.1:p.Gly541Ala
XM_011545997.1:c.2830-3542C>G (RNF40)	XP_011544299.1:n.2830-3542C>G
XM_011545997.2:c.2830-3542C>G (RNF40)	XP_011544299.1:n.2830-3542C>G
XM_011545998.1:c.2830-3542C>G (RNF40)	XP_011544300.1:n.2830-3542C>G
XM_011545999.1:c.2830-3542C>G (RNF40)	XP_011544301.1:n.2830-3542C>G