Canonical Allele Identifier: CA396600844

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70882863C>A , CM000678.2:g.70882863C>A	GRCh38
NC_000016.9:g.70916766C>A , CM000678.1:g.70916766C>A	GRCh37
NG_033116.1:g.352860G>T
NG_033116.2:g.352860G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001270974.2:c.10012G>T MANE Select	NP_001257903.1:p.Glu3338Ter
ENST00000393567.7:c.10012G>T MANE Select	ENSP00000377197.2:p.Glu3338Ter
NM_001270974.1:c.10012G>T	NP_001257903.1:p.Glu3338Ter
ENST00000393567.6:c.10012G>T	ENSP00000377197.2:p.Glu3338Ter
XM_006721206.2:c.10063G>T	XP_006721269.1:p.Glu3355Ter
XM_006721206.3:c.10063G>T	XP_006721269.1:p.Glu3355Ter
XM_011523146.1:c.10195G>T	XP_011521448.1:p.Glu3399Ter
XM_011523146.2:c.10195G>T	XP_011521448.1:p.Glu3399Ter
XM_011523147.1:c.10165G>T	XP_011521449.1:p.Glu3389Ter
XM_011523148.1:c.10114G>T	XP_011521450.1:p.Glu3372Ter
XM_011523149.1:c.10114G>T	XP_011521451.1:p.Glu3372Ter
XM_011523150.1:c.10114G>T	XP_011521452.1:p.Glu3372Ter
XM_011523151.1:c.10093G>T	XP_011521453.1:p.Glu3365Ter
XM_011523151.2:c.10093G>T	XP_011521453.1:p.Glu3365Ter
XM_011523152.1:c.3874G>T	XP_011521454.1:p.Glu1292Ter
XM_011523153.1:c.3400G>T	XP_011521455.1:p.Glu1134Ter
XM_011523154.1:c.2992G>T	XP_011521456.1:p.Glu998Ter
XM_011523155.1:c.2902G>T	XP_011521457.1:p.Glu968Ter
XM_011523155.2:c.2902G>T	XP_011521457.1:p.Glu968Ter
XM_017023346.2:c.10132G>T	XP_016878835.1:p.Glu3378Ter
XM_017023347.1:c.8224G>T	XP_016878836.1:p.Glu2742Ter
XM_017023348.1:c.8224G>T	XP_016878837.1:p.Glu2742Ter