Canonical Allele Identifier: CA396599019

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70879725A>C , CM000678.2:g.70879725A>C	GRCh38
NC_000016.9:g.70913628A>C , CM000678.1:g.70913628A>C	GRCh37
NG_033116.1:g.355998T>G
NG_033116.2:g.355998T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001270974.2:c.10247T>G MANE Select	NP_001257903.1:p.Val3416Gly
ENST00000393567.7:c.10247T>G MANE Select	ENSP00000377197.2:p.Val3416Gly
NM_001270974.1:c.10247T>G	NP_001257903.1:p.Val3416Gly
ENST00000393567.6:c.10247T>G	ENSP00000377197.2:p.Val3416Gly
XM_006721206.2:c.10298T>G	XP_006721269.1:p.Val3433Gly
XM_006721206.3:c.10298T>G	XP_006721269.1:p.Val3433Gly
XM_011523146.1:c.10430T>G	XP_011521448.1:p.Val3477Gly
XM_011523146.2:c.10430T>G	XP_011521448.1:p.Val3477Gly
XM_011523147.1:c.10400T>G	XP_011521449.1:p.Val3467Gly
XM_011523148.1:c.10349T>G	XP_011521450.1:p.Val3450Gly
XM_011523149.1:c.10349T>G	XP_011521451.1:p.Val3450Gly
XM_011523150.1:c.10349T>G	XP_011521452.1:p.Val3450Gly
XM_011523151.1:c.10328T>G	XP_011521453.1:p.Val3443Gly
XM_011523151.2:c.10328T>G	XP_011521453.1:p.Val3443Gly
XM_011523152.1:c.4109T>G	XP_011521454.1:p.Val1370Gly
XM_011523153.1:c.3635T>G	XP_011521455.1:p.Val1212Gly
XM_011523154.1:c.3227T>G	XP_011521456.1:p.Val1076Gly
XM_011523155.1:c.3137T>G	XP_011521457.1:p.Val1046Gly
XM_011523155.2:c.3137T>G	XP_011521457.1:p.Val1046Gly
XM_017023346.2:c.10367T>G	XP_016878835.1:p.Val3456Gly
XM_017023347.1:c.8459T>G	XP_016878836.1:p.Val2820Gly
XM_017023348.1:c.8459T>G	XP_016878837.1:p.Val2820Gly