Canonical Allele Identifier: CA396595193

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70834166T>C , CM000678.2:g.70834166T>C	GRCh38
NC_000016.9:g.70868069T>C , CM000678.1:g.70868069T>C	GRCh37
NG_033116.1:g.401557A>G
NG_033116.2:g.401557A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001270974.2:c.13402-2A>G MANE Select	NP_001257903.1:n.13402-2A>G
ENST00000393567.7:c.13402-2A>G MANE Select	ENSP00000377197.2:n.13402-2A>G
NM_001270974.1:c.13402-2A>G	NP_001257903.1:n.13402-2A>G
ENST00000378856.8:c.2306-2A>G
ENST00000393567.6:c.13402-2A>G	ENSP00000377197.2:n.13402-2A>G
XM_006721206.2:c.13453-2A>G	XP_006721269.1:n.13453-2A>G
XM_006721206.3:c.13453-2A>G	XP_006721269.1:n.13453-2A>G
XM_011523146.1:c.13585-2A>G	XP_011521448.1:n.13585-2A>G
XM_011523146.2:c.13585-2A>G	XP_011521448.1:n.13585-2A>G
XM_011523147.1:c.13555-2A>G	XP_011521449.1:n.13555-2A>G
XM_011523148.1:c.13504-2A>G	XP_011521450.1:n.13504-2A>G
XM_011523149.1:c.13504-2A>G	XP_011521451.1:n.13504-2A>G
XM_011523150.1:c.13504-2A>G	XP_011521452.1:n.13504-2A>G
XM_011523151.1:c.13483-2A>G	XP_011521453.1:n.13483-2A>G
XM_011523151.2:c.13483-2A>G	XP_011521453.1:n.13483-2A>G
XM_011523152.1:c.7264-2A>G	XP_011521454.1:n.7264-2A>G
XM_011523153.1:c.6790-2A>G	XP_011521455.1:n.6790-2A>G
XM_011523154.1:c.6382-2A>G	XP_011521456.1:n.6382-2A>G
XM_011523155.1:c.6292-2A>G	XP_011521457.1:n.6292-2A>G
XM_011523155.2:c.6292-2A>G	XP_011521457.1:n.6292-2A>G
XM_017023346.2:c.13522-2A>G	XP_016878835.1:n.13522-2A>G
XM_017023347.1:c.11614-2A>G	XP_016878836.1:n.11614-2A>G
XM_017023348.1:c.11614-2A>G	XP_016878837.1:n.11614-2A>G