Canonical Allele Identifier: CA396609672

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70901189C>T , CM000678.2:g.70901189C>T	GRCh38
NC_000016.9:g.70935092C>T , CM000678.1:g.70935092C>T	GRCh37
NG_033116.1:g.334534G>A
NG_033116.2:g.334534G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393567.7:c.8863G>A MANE Select	ENSP00000377197.2:p.Val2955Ile
ENST00000309900.11:n.3316G>A
ENST00000393567.6:c.8863G>A	ENSP00000377197.2:p.Val2955Ile
NM_001270974.1:c.8863G>A	NP_001257903.1:p.Val2955Ile
XM_006721206.2:c.8914G>A	XP_006721269.1:p.Val2972Ile
XM_011523146.1:c.9046G>A	XP_011521448.1:p.Val3016Ile
XM_011523147.1:c.9016G>A	XP_011521449.1:p.Val3006Ile
XM_011523148.1:c.8965G>A	XP_011521450.1:p.Val2989Ile
XM_011523149.1:c.8965G>A	XP_011521451.1:p.Val2989Ile
XM_011523150.1:c.8965G>A	XP_011521452.1:p.Val2989Ile
XM_011523151.1:c.8944G>A	XP_011521453.1:p.Val2982Ile
XM_011523152.1:c.2725G>A	XP_011521454.1:p.Val909Ile
XM_011523153.1:c.2251G>A	XP_011521455.1:p.Val751Ile
XM_011523154.1:c.1843G>A	XP_011521456.1:p.Val615Ile
XM_011523155.1:c.1753G>A	XP_011521457.1:p.Val585Ile
NM_001270974.2:c.8863G>A MANE Select	NP_001257903.1:p.Val2955Ile
XM_006721206.3:c.8914G>A	XP_006721269.1:p.Val2972Ile
XM_011523146.2:c.9046G>A	XP_011521448.1:p.Val3016Ile
XM_011523151.2:c.8944G>A	XP_011521453.1:p.Val2982Ile
XM_011523155.2:c.1753G>A	XP_011521457.1:p.Val585Ile
XM_017023346.2:c.8983G>A	XP_016878835.1:p.Val2995Ile
XM_017023347.1:c.7075G>A	XP_016878836.1:p.Val2359Ile
XM_017023348.1:c.7075G>A	XP_016878837.1:p.Val2359Ile