Canonical Allele Identifier: CA8148955

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70862187C>T , CM000678.2:g.70862187C>T	GRCh38
NC_000016.9:g.70896090C>T , CM000678.1:g.70896090C>T	GRCh37
NG_033116.1:g.373536G>A
NG_033116.2:g.373536G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001270974.2:c.11638G>A MANE Select	NP_001257903.1:p.Asp3880Asn
ENST00000393567.7:c.11638G>A MANE Select	ENSP00000377197.2:p.Asp3880Asn
NM_001270974.1:c.11638G>A	NP_001257903.1:p.Asp3880Asn
ENST00000378856.8:c.542G>A
ENST00000393567.6:c.11638G>A	ENSP00000377197.2:p.Asp3880Asn
ENST00000546257.1:c.86+898G>A
XM_006721206.2:c.11689G>A	XP_006721269.1:p.Asp3897Asn
XM_006721206.3:c.11689G>A	XP_006721269.1:p.Asp3897Asn
XM_011523146.1:c.11821G>A	XP_011521448.1:p.Asp3941Asn
XM_011523146.2:c.11821G>A	XP_011521448.1:p.Asp3941Asn
XM_011523147.1:c.11791G>A	XP_011521449.1:p.Asp3931Asn
XM_011523148.1:c.11740G>A	XP_011521450.1:p.Asp3914Asn
XM_011523149.1:c.11740G>A	XP_011521451.1:p.Asp3914Asn
XM_011523150.1:c.11740G>A	XP_011521452.1:p.Asp3914Asn
XM_011523151.1:c.11719G>A	XP_011521453.1:p.Asp3907Asn
XM_011523151.2:c.11719G>A	XP_011521453.1:p.Asp3907Asn
XM_011523152.1:c.5500G>A	XP_011521454.1:p.Asp1834Asn
XM_011523153.1:c.5026G>A	XP_011521455.1:p.Asp1676Asn
XM_011523154.1:c.4618G>A	XP_011521456.1:p.Asp1540Asn
XM_011523155.1:c.4528G>A	XP_011521457.1:p.Asp1510Asn
XM_011523155.2:c.4528G>A	XP_011521457.1:p.Asp1510Asn
XM_017023346.2:c.11758G>A	XP_016878835.1:p.Asp3920Asn
XM_017023347.1:c.9850G>A	XP_016878836.1:p.Asp3284Asn
XM_017023348.1:c.9850G>A	XP_016878837.1:p.Asp3284Asn