Canonical Allele Identifier: CA2001153451

Gene: ANKK1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113400025_113400048delinsCACGCCCGCAACAAGGTGGGCTGG , CM000673.2:g.113400025_113400048delinsCACGCCCGCAACAAGGTGGGCTGG	GRCh38
NC_000011.9:g.113270747_113270770delinsCACGCCCGCAACAAGGTGGGCTGG , CM000673.1:g.113270747_113270770delinsCACGCCCGCAACAAGGTGGGCTGG	GRCh37
NC_000011.8:g.112775957_112775980delinsCACGCCCGCAACAAGGTGGGCTGG	NCBI36
NG_012976.1:g.17235_17258delinsCACGCCCGCAACAAGGTGGGCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303941.4:c.2056_2079delinsCACGCCCGCAACAAGGTGGGCTGG MANE Select	ENSP00000306678.3:p.His686=
ENST00000303941.3:c.2056_2079delinsCACGCCCGCAACAAGGTGGGCTGG	ENSP00000306678.3:p.His686=
NM_178510.1:c.2056_2079delinsCACGCCCGCAACAAGGTGGGCTGG	NP_848605.1:p.His686=
XM_011542736.1:c.2089_2112delinsCACGCCCGCAACAAGGTGGGCTGG	XP_011541038.1:p.His697=
XM_011542737.1:c.2059_2082delinsCACGCCCGCAACAAGGTGGGCTGG	XP_011541039.1:p.His687=
XM_011542738.1:c.1867_1890delinsCACGCCCGCAACAAGGTGGGCTGG	XP_011541040.1:p.His623=
XM_011542736.2:c.2089_2112delinsCACGCCCGCAACAAGGTGGGCTGG	XP_011541038.1:p.His697=
XM_011542737.2:c.2059_2082delinsCACGCCCGCAACAAGGTGGGCTGG	XP_011541039.1:p.His687=
XM_011542738.2:c.1867_1890delinsCACGCCCGCAACAAGGTGGGCTGG	XP_011541040.1:p.His623=
XM_017017475.1:c.2086_2109delinsCACGCCCGCAACAAGGTGGGCTGG	XP_016872964.1:p.His696=
NM_178510.2:c.2056_2079delinsCACGCCCGCAACAAGGTGGGCTGG MANE Select	NP_848605.1:p.His686=