Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.115413875_115413876delinsAG , CM000670.2:g.115413875_115413876delinsAG	GRCh38
NC_000008.10:g.116426103_116426104delinsAG , CM000670.1:g.116426103_116426104delinsAG	GRCh37
NC_000008.9:g.116495279_116495280delinsAG	NCBI36
NG_012383.3:g.260126_260127delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395715.8:c.147_148delinsCT MANE Select	ENSP00000379065.3:n.147_148delinsCT
ENST00000640765.1:c.147_148delinsCT	ENSP00000492037.1:n.147_148delinsCT
ENST00000220888.9:c.147_148delinsCT	ENSP00000220888.5:n.147_148delinsCT
ENST00000395715.7:c.147_148delinsCT	ENSP00000379065.3:n.147_148delinsCT
ENST00000519076.5:c.147_148delinsCT	ENSP00000428910.1:n.147_148delinsCT
NM_001282902.2:c.147_148delinsCT	NP_001269831.1:n.147_148delinsCT
NM_001282903.2:c.147_148delinsCT	NP_001269832.1:n.147_148delinsCT
NM_014112.4:c.147_148delinsCT	NP_054831.2:n.147_148delinsCT
XM_005251049.2:c.147_148delinsCT	XP_005251106.1:n.147_148delinsCT
XM_006716625.1:c.147_148delinsCT	XP_006716688.1:n.147_148delinsCT
XM_011517264.1:c.147_148delinsCT	XP_011515566.1:n.147_148delinsCT
XM_011517265.1:c.147_148delinsCT	XP_011515567.1:n.147_148delinsCT
XM_011517266.1:c.147_148delinsCT	XP_011515568.1:n.147_148delinsCT
XM_011517267.1:c.147_148delinsCT	XP_011515569.1:n.147_148delinsCT
XM_011517268.1:c.147_148delinsCT	XP_011515570.1:n.147_148delinsCT
NM_001330599.1:c.147_148delinsCT	NP_001317528.1:n.147_148delinsCT
XM_011517264.2:c.147_148delinsCT	XP_011515566.1:n.147_148delinsCT
XM_011517266.3:c.147_148delinsCT	XP_011515568.1:n.147_148delinsCT
XM_011517268.2:c.147_148delinsCT	XP_011515570.1:n.147_148delinsCT
NM_001282902.3:c.147_148delinsCT	NP_001269831.1:n.147_148delinsCT
NM_001282903.3:c.147_148delinsCT	NP_001269832.1:n.147_148delinsCT
NM_001330599.2:c.147_148delinsCT	NP_001317528.1:n.147_148delinsCT
NM_014112.5:c.147_148delinsCT MANE Select	NP_054831.2:n.147_148delinsCT

HGVS	Amino-acid Change
ENST00000395715.8:c.147_148delinsCT MANE Select	ENSP00000379065.3:n.147_148delinsCT
ENST00000640765.1:c.147_148delinsCT	ENSP00000492037.1:n.147_148delinsCT
ENST00000220888.9:c.147_148delinsCT	ENSP00000220888.5:n.147_148delinsCT
ENST00000395715.7:c.147_148delinsCT	ENSP00000379065.3:n.147_148delinsCT
ENST00000519076.5:c.147_148delinsCT	ENSP00000428910.1:n.147_148delinsCT
NM_001282902.2:c.147_148delinsCT	NP_001269831.1:n.147_148delinsCT
NM_001282903.2:c.147_148delinsCT	NP_001269832.1:n.147_148delinsCT
NM_014112.4:c.147_148delinsCT	NP_054831.2:n.147_148delinsCT
XM_005251049.2:c.147_148delinsCT	XP_005251106.1:n.147_148delinsCT
XM_006716625.1:c.147_148delinsCT	XP_006716688.1:n.147_148delinsCT
XM_011517264.1:c.147_148delinsCT	XP_011515566.1:n.147_148delinsCT
XM_011517265.1:c.147_148delinsCT	XP_011515567.1:n.147_148delinsCT
XM_011517266.1:c.147_148delinsCT	XP_011515568.1:n.147_148delinsCT
XM_011517267.1:c.147_148delinsCT	XP_011515569.1:n.147_148delinsCT
XM_011517268.1:c.147_148delinsCT	XP_011515570.1:n.147_148delinsCT
NM_001330599.1:c.147_148delinsCT	NP_001317528.1:n.147_148delinsCT
XM_011517264.2:c.147_148delinsCT	XP_011515566.1:n.147_148delinsCT
XM_011517266.3:c.147_148delinsCT	XP_011515568.1:n.147_148delinsCT
XM_011517268.2:c.147_148delinsCT	XP_011515570.1:n.147_148delinsCT
NM_001282902.3:c.147_148delinsCT	NP_001269831.1:n.147_148delinsCT
NM_001282903.3:c.147_148delinsCT	NP_001269832.1:n.147_148delinsCT
NM_001330599.2:c.147_148delinsCT	NP_001317528.1:n.147_148delinsCT
NM_014112.5:c.147_148delinsCT MANE Select	NP_054831.2:n.147_148delinsCT