Canonical Allele Identifier: CA8150212

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70943811C>T , CM000678.2:g.70943811C>T	GRCh38
NC_000016.9:g.70977714C>T , CM000678.1:g.70977714C>T	GRCh37
NG_033116.1:g.291912G>A
NG_033116.2:g.291912G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001270974.2:c.6669+1G>A MANE Select	NP_001257903.1:n.6669+1G>A
ENST00000393567.7:c.6669+1G>A MANE Select	ENSP00000377197.2:n.6669+1G>A
NM_001270974.1:c.6669+1G>A	NP_001257903.1:n.6669+1G>A
ENST00000309900.11:n.1190-1992G>A
ENST00000393567.6:c.6669+1G>A	ENSP00000377197.2:n.6669+1G>A
ENST00000543521.1:n.1444-1992G>A
XM_006721206.2:c.6720+1G>A	XP_006721269.1:n.6720+1G>A
XM_006721206.3:c.6720+1G>A	XP_006721269.1:n.6720+1G>A
XM_011523146.1:c.6852+1G>A	XP_011521448.1:n.6852+1G>A
XM_011523146.2:c.6852+1G>A	XP_011521448.1:n.6852+1G>A
XM_011523147.1:c.6822+1G>A	XP_011521449.1:n.6822+1G>A
XM_011523148.1:c.6771+1G>A	XP_011521450.1:n.6771+1G>A
XM_011523149.1:c.6771+1G>A	XP_011521451.1:n.6771+1G>A
XM_011523150.1:c.6771+1G>A	XP_011521452.1:n.6771+1G>A
XM_011523151.1:c.6750+1G>A	XP_011521453.1:n.6750+1G>A
XM_011523151.2:c.6750+1G>A	XP_011521453.1:n.6750+1G>A
XM_011523152.1:c.531+1G>A	XP_011521454.1:n.531+1G>A
XM_011523153.1:c.57+1G>A	XP_011521455.1:n.57+1G>A
XM_017023346.2:c.6789+1G>A	XP_016878835.1:n.6789+1G>A
XM_017023347.1:c.4881+1G>A	XP_016878836.1:n.4881+1G>A
XM_017023348.1:c.4881+1G>A	XP_016878837.1:n.4881+1G>A