Canonical Allele Identifier: CA396611932

Gene: HYDIN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70872181T>C , CM000678.2:g.70872181T>C	GRCh38
NC_000016.9:g.70906084T>C , CM000678.1:g.70906084T>C	GRCh37
NG_033116.1:g.363542A>G
NG_033116.2:g.363542A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001270974.2:c.10949-2A>G MANE Select	NP_001257903.1:n.10949-2A>G
ENST00000393567.7:c.10949-2A>G MANE Select	ENSP00000377197.2:n.10949-2A>G
NM_001270974.1:c.10949-2A>G	NP_001257903.1:n.10949-2A>G
ENST00000393567.6:c.10949-2A>G	ENSP00000377197.2:n.10949-2A>G
XM_006721206.2:c.11000-2A>G	XP_006721269.1:n.11000-2A>G
XM_006721206.3:c.11000-2A>G	XP_006721269.1:n.11000-2A>G
XM_011523146.1:c.11132-2A>G	XP_011521448.1:n.11132-2A>G
XM_011523146.2:c.11132-2A>G	XP_011521448.1:n.11132-2A>G
XM_011523147.1:c.11102-2A>G	XP_011521449.1:n.11102-2A>G
XM_011523148.1:c.11051-2A>G	XP_011521450.1:n.11051-2A>G
XM_011523149.1:c.11051-2A>G	XP_011521451.1:n.11051-2A>G
XM_011523150.1:c.11051-2A>G	XP_011521452.1:n.11051-2A>G
XM_011523151.1:c.11030-2A>G	XP_011521453.1:n.11030-2A>G
XM_011523151.2:c.11030-2A>G	XP_011521453.1:n.11030-2A>G
XM_011523152.1:c.4811-2A>G	XP_011521454.1:n.4811-2A>G
XM_011523153.1:c.4337-2A>G	XP_011521455.1:n.4337-2A>G
XM_011523154.1:c.3929-2A>G	XP_011521456.1:n.3929-2A>G
XM_011523155.1:c.3839-2A>G	XP_011521457.1:n.3839-2A>G
XM_011523155.2:c.3839-2A>G	XP_011521457.1:n.3839-2A>G
XM_017023346.2:c.11069-2A>G	XP_016878835.1:n.11069-2A>G
XM_017023347.1:c.9161-2A>G	XP_016878836.1:n.9161-2A>G
XM_017023348.1:c.9161-2A>G	XP_016878837.1:n.9161-2A>G