Canonical Allele Identifier: CA1694185008

Gene: HYCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22945391A>T , CM000669.2:g.22945391A>T	GRCh38
NC_000007.13:g.22985010A>T , CM000669.1:g.22985010A>T	GRCh37
NC_000007.12:g.22951535A>T	NCBI36
NG_008392.1:g.73761T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032581.4:c.*198T>A MANE Select	NP_115970.2:n.*198T>A
ENST00000432176.7:c.*198T>A MANE Select	ENSP00000403396.2:n.*198T>A
NM_001363466.1:c.*800T>A	NP_001350395.1:n.*800T>A
NM_001363466.2:c.*800T>A	NP_001350395.1:n.*800T>A
NM_001363467.1:c.*758T>A	NP_001350396.1:n.*758T>A
NM_001363467.2:c.*758T>A	NP_001350396.1:n.*758T>A
NM_032581.3:c.*198T>A	NP_115970.2:n.*198T>A
ENST00000409923.5:c.*800T>A	ENSP00000386246.1:n.*800T>A
ENST00000432176.6:c.*198T>A	ENSP00000403396.2:n.*198T>A
ENST00000440481.5:c.2215T>A
ENST00000440481.6:c.*800T>A	ENSP00000397168.2:n.*800T>A
ENST00000465661.2:n.1182+14865T>A
ENST00000679789.1:c.*917T>A	ENSP00000506308.1:n.*917T>A
ENST00000679826.1:c.*198T>A	ENSP00000505460.1:n.*198T>A
ENST00000680721.1:n.1787T>A
ENST00000681237.1:c.*1420T>A	ENSP00000505270.1:n.*1420T>A
ENST00000681402.1:c.*1474T>A	ENSP00000506692.1:n.*1474T>A
ENST00000681766.1:c.*198T>A	ENSP00000505161.1:n.*198T>A
XM_005249894.3:c.*800T>A	XP_005249951.1:n.*800T>A
XM_006715799.2:c.*198T>A	XP_006715862.1:n.*198T>A
XM_011515589.1:c.*198T>A	XP_011513891.1:n.*198T>A
XM_011515589.2:c.*198T>A	XP_011513891.1:n.*198T>A
XM_011515590.1:c.991+14865T>A	XP_011513892.1:n.991+14865T>A
XM_011515590.2:c.991+14865T>A	XP_011513892.1:n.991+14865T>A