Canonical Allele Identifier: CA8151612

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.71178936T>A , CM000678.2:g.71178936T>A	GRCh38
NC_000016.9:g.71212839T>A , CM000678.1:g.71212839T>A	GRCh37
NC_000016.8:g.69770340T>A	NCBI36
NG_033116.1:g.56787A>T
NG_033116.2:g.56787A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001270974.2:c.373A>T MANE Select	NP_001257903.1:p.Asn125Tyr
ENST00000393567.7:c.373A>T MANE Select	ENSP00000377197.2:p.Asn125Tyr
NM_001198542.1:c.454A>T	NP_001185471.1:p.Asn152Tyr
NM_001198543.1:c.424A>T	NP_001185472.1:p.Asn142Tyr
NM_001270974.1:c.373A>T	NP_001257903.1:p.Asn125Tyr
NM_017558.4:c.373A>T	NP_060028.2:p.Asn125Tyr
NM_017558.5:c.373A>T	NP_060028.2:p.Asn125Tyr
ENST00000288168.14:c.424A>T	ENSP00000288168.10:p.Asn142Tyr
ENST00000321489.9:c.373A>T	ENSP00000314736.5:p.Asn125Tyr
ENST00000393567.6:c.373A>T	ENSP00000377197.2:p.Asn125Tyr
ENST00000537789.1:n.91A>T
ENST00000538248.5:c.454A>T	ENSP00000444970.1:p.Asn152Tyr
ENST00000539447.5:c.276A>T
ENST00000541601.5:c.424A>T	ENSP00000437341.1:p.Asn142Tyr
XM_006721206.2:c.424A>T	XP_006721269.1:p.Asn142Tyr
XM_006721206.3:c.424A>T	XP_006721269.1:p.Asn142Tyr
XM_011523146.1:c.454A>T	XP_011521448.1:p.Asn152Tyr
XM_011523146.2:c.454A>T	XP_011521448.1:p.Asn152Tyr
XM_011523147.1:c.424A>T	XP_011521449.1:p.Asn142Tyr
XM_011523148.1:c.373A>T	XP_011521450.1:p.Asn125Tyr
XM_011523149.1:c.373A>T	XP_011521451.1:p.Asn125Tyr
XM_011523150.1:c.373A>T	XP_011521452.1:p.Asn125Tyr
XM_011523151.1:c.454A>T	XP_011521453.1:p.Asn152Tyr
XM_011523151.2:c.454A>T	XP_011521453.1:p.Asn152Tyr
XM_017023346.2:c.493A>T	XP_016878835.1:p.Asn165Tyr