Canonical Allele Identifier: CA396601109

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70850656C>T , CM000678.2:g.70850656C>T	GRCh38
NC_000016.9:g.70884559C>T , CM000678.1:g.70884559C>T	GRCh37
NG_033116.1:g.385067G>A
NG_033116.2:g.385067G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001270974.2:c.12444-1G>A MANE Select	NP_001257903.1:n.12444-1G>A
ENST00000393567.7:c.12444-1G>A MANE Select	ENSP00000377197.2:n.12444-1G>A
NM_001270974.1:c.12444-1G>A	NP_001257903.1:n.12444-1G>A
ENST00000378856.8:c.1348-1G>A
ENST00000393567.6:c.12444-1G>A	ENSP00000377197.2:n.12444-1G>A
XM_006721206.2:c.12495-1G>A	XP_006721269.1:n.12495-1G>A
XM_006721206.3:c.12495-1G>A	XP_006721269.1:n.12495-1G>A
XM_011523146.1:c.12627-1G>A	XP_011521448.1:n.12627-1G>A
XM_011523146.2:c.12627-1G>A	XP_011521448.1:n.12627-1G>A
XM_011523147.1:c.12597-1G>A	XP_011521449.1:n.12597-1G>A
XM_011523148.1:c.12546-1G>A	XP_011521450.1:n.12546-1G>A
XM_011523149.1:c.12546-1G>A	XP_011521451.1:n.12546-1G>A
XM_011523150.1:c.12546-1G>A	XP_011521452.1:n.12546-1G>A
XM_011523151.1:c.12525-1G>A	XP_011521453.1:n.12525-1G>A
XM_011523151.2:c.12525-1G>A	XP_011521453.1:n.12525-1G>A
XM_011523152.1:c.6306-1G>A	XP_011521454.1:n.6306-1G>A
XM_011523153.1:c.5832-1G>A	XP_011521455.1:n.5832-1G>A
XM_011523154.1:c.5424-1G>A	XP_011521456.1:n.5424-1G>A
XM_011523155.1:c.5334-1G>A	XP_011521457.1:n.5334-1G>A
XM_011523155.2:c.5334-1G>A	XP_011521457.1:n.5334-1G>A
XM_017023346.2:c.12564-1G>A	XP_016878835.1:n.12564-1G>A
XM_017023347.1:c.10656-1G>A	XP_016878836.1:n.10656-1G>A
XM_017023348.1:c.10656-1G>A	XP_016878837.1:n.10656-1G>A