Canonical Allele Identifier: CA8149576

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70894474G>A , CM000678.2:g.70894474G>A	GRCh38
NC_000016.9:g.70928377G>A , CM000678.1:g.70928377G>A	GRCh37
NG_033116.1:g.341249C>T
NG_033116.2:g.341249C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001270974.2:c.9223C>T MANE Select	NP_001257903.1:p.Arg3075Cys
ENST00000393567.7:c.9223C>T MANE Select	ENSP00000377197.2:p.Arg3075Cys
NM_001270974.1:c.9223C>T	NP_001257903.1:p.Arg3075Cys
ENST00000309900.11:n.3676C>T
ENST00000393567.6:c.9223C>T	ENSP00000377197.2:p.Arg3075Cys
XM_006721206.2:c.9274C>T	XP_006721269.1:p.Arg3092Cys
XM_006721206.3:c.9274C>T	XP_006721269.1:p.Arg3092Cys
XM_011523146.1:c.9406C>T	XP_011521448.1:p.Arg3136Cys
XM_011523146.2:c.9406C>T	XP_011521448.1:p.Arg3136Cys
XM_011523147.1:c.9376C>T	XP_011521449.1:p.Arg3126Cys
XM_011523148.1:c.9325C>T	XP_011521450.1:p.Arg3109Cys
XM_011523149.1:c.9325C>T	XP_011521451.1:p.Arg3109Cys
XM_011523150.1:c.9325C>T	XP_011521452.1:p.Arg3109Cys
XM_011523151.1:c.9304C>T	XP_011521453.1:p.Arg3102Cys
XM_011523151.2:c.9304C>T	XP_011521453.1:p.Arg3102Cys
XM_011523152.1:c.3085C>T	XP_011521454.1:p.Arg1029Cys
XM_011523153.1:c.2611C>T	XP_011521455.1:p.Arg871Cys
XM_011523154.1:c.2203C>T	XP_011521456.1:p.Arg735Cys
XM_011523155.1:c.2113C>T	XP_011521457.1:p.Arg705Cys
XM_011523155.2:c.2113C>T	XP_011521457.1:p.Arg705Cys
XM_017023346.2:c.9343C>T	XP_016878835.1:p.Arg3115Cys
XM_017023347.1:c.7435C>T	XP_016878836.1:p.Arg2479Cys
XM_017023348.1:c.7435C>T	XP_016878837.1:p.Arg2479Cys