Canonical Allele Identifier: CA8150325

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70955402G>A , CM000678.2:g.70955402G>A	GRCh38
NC_000016.9:g.70989305G>A , CM000678.1:g.70989305G>A	GRCh37
NG_033116.1:g.280321C>T
NG_033116.2:g.280321C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001270974.2:c.6289C>T MANE Select	NP_001257903.1:p.Gln2097Ter
ENST00000393567.7:c.6289C>T MANE Select	ENSP00000377197.2:p.Gln2097Ter
NM_001270974.1:c.6289C>T	NP_001257903.1:p.Gln2097Ter
ENST00000309900.11:n.1162C>T
ENST00000393567.6:c.6289C>T	ENSP00000377197.2:p.Gln2097Ter
ENST00000543521.1:n.1416C>T
XM_006721206.2:c.6340C>T	XP_006721269.1:p.Gln2114Ter
XM_006721206.3:c.6340C>T	XP_006721269.1:p.Gln2114Ter
XM_011523146.1:c.6472C>T	XP_011521448.1:p.Gln2158Ter
XM_011523146.2:c.6472C>T	XP_011521448.1:p.Gln2158Ter
XM_011523147.1:c.6442C>T	XP_011521449.1:p.Gln2148Ter
XM_011523148.1:c.6391C>T	XP_011521450.1:p.Gln2131Ter
XM_011523149.1:c.6391C>T	XP_011521451.1:p.Gln2131Ter
XM_011523150.1:c.6391C>T	XP_011521452.1:p.Gln2131Ter
XM_011523151.1:c.6370C>T	XP_011521453.1:p.Gln2124Ter
XM_011523151.2:c.6370C>T	XP_011521453.1:p.Gln2124Ter
XM_011523152.1:c.151C>T	XP_011521454.1:p.Gln51Ter
XM_017023346.2:c.6409C>T	XP_016878835.1:p.Gln2137Ter
XM_017023347.1:c.4501C>T	XP_016878836.1:p.Gln1501Ter
XM_017023348.1:c.4501C>T	XP_016878837.1:p.Gln1501Ter