Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110617464_110617465insA , CM000666.2:g.110617464_110617465insA	GRCh38
NC_000004.11:g.111538620_111538621insA , CM000666.1:g.111538620_111538621insA	GRCh37
NC_000004.10:g.111758069_111758070insA	NCBI36
NG_007120.1:g.24888_24889insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613094.5:c.883_884insT	ENSP00000484763.2:n.883_884insT
ENST00000614423.5:c.660_661insT	ENSP00000481951.2:n.660_661insT
ENST00000394595.8:c.660_661insT	ENSP00000378095.4:n.660_661insT
ENST00000644488.1:n.1677_1678insT
ENST00000644743.1:c.660_661insT MANE Select	ENSP00000495061.1:n.660_661insT
ENST00000645131.1:n.1566_1567insT
ENST00000306732.7:c.660_661insT	ENSP00000304169.3:n.660_661insT
ENST00000354925.6:c.660_661insT	ENSP00000347004.2:n.660_661insT
ENST00000355080.9:c.660_661insT	ENSP00000347192.5:n.660_661insT
ENST00000394595.7:c.883_884insT	ENSP00000378095.3:n.883_884insT
ENST00000394598.6:c.660_661insT	ENSP00000378097.2:n.660_661insT
ENST00000607868.1:n.1362_1363insT
ENST00000613094.4:c.660_661insT	ENSP00000484763.1:n.660_661insT
ENST00000614423.4:c.660_661insT	ENSP00000481951.1:n.660_661insT
ENST00000616641.4:c.660_661insT	ENSP00000484909.1:n.660_661insT
NM_000325.5:c.660_661insT	NP_000316.2:n.660_661insT
NM_001204397.1:c.660_661insT	NP_001191326.1:n.660_661insT
NM_001204398.1:c.660_661insT	NP_001191327.1:n.660_661insT
NM_001204399.1:c.660_661insT	NP_001191328.1:n.660_661insT
NM_153426.2:c.660_661insT	NP_700475.1:n.660_661insT
NM_153427.2:c.660_661insT	NP_700476.1:n.660_661insT
XM_006714235.2:c.660_661insT	XP_006714298.1:n.660_661insT
XM_011532027.1:c.660_661insT	XP_011530329.1:n.660_661insT
XM_024454090.1:c.660_661insT	XP_024309858.1:n.660_661insT
NM_000325.6:c.660_661insT MANE Select	NP_000316.2:n.660_661insT
NM_001204397.2:c.660_661insT	NP_001191326.1:n.660_661insT
NM_153426.3:c.660_661insT	NP_700475.1:n.660_661insT
NM_153427.3:c.660_661insT	NP_700476.1:n.660_661insT

HGVS	Amino-acid Change
ENST00000613094.5:c.883_884insT	ENSP00000484763.2:n.883_884insT
ENST00000614423.5:c.660_661insT	ENSP00000481951.2:n.660_661insT
ENST00000394595.8:c.660_661insT	ENSP00000378095.4:n.660_661insT
ENST00000644488.1:n.1677_1678insT
ENST00000644743.1:c.660_661insT MANE Select	ENSP00000495061.1:n.660_661insT
ENST00000645131.1:n.1566_1567insT
ENST00000306732.7:c.660_661insT	ENSP00000304169.3:n.660_661insT
ENST00000354925.6:c.660_661insT	ENSP00000347004.2:n.660_661insT
ENST00000355080.9:c.660_661insT	ENSP00000347192.5:n.660_661insT
ENST00000394595.7:c.883_884insT	ENSP00000378095.3:n.883_884insT
ENST00000394598.6:c.660_661insT	ENSP00000378097.2:n.660_661insT
ENST00000607868.1:n.1362_1363insT
ENST00000613094.4:c.660_661insT	ENSP00000484763.1:n.660_661insT
ENST00000614423.4:c.660_661insT	ENSP00000481951.1:n.660_661insT
ENST00000616641.4:c.660_661insT	ENSP00000484909.1:n.660_661insT
NM_000325.5:c.660_661insT	NP_000316.2:n.660_661insT
NM_001204397.1:c.660_661insT	NP_001191326.1:n.660_661insT
NM_001204398.1:c.660_661insT	NP_001191327.1:n.660_661insT
NM_001204399.1:c.660_661insT	NP_001191328.1:n.660_661insT
NM_153426.2:c.660_661insT	NP_700475.1:n.660_661insT
NM_153427.2:c.660_661insT	NP_700476.1:n.660_661insT
XM_006714235.2:c.660_661insT	XP_006714298.1:n.660_661insT
XM_011532027.1:c.660_661insT	XP_011530329.1:n.660_661insT
XM_024454090.1:c.660_661insT	XP_024309858.1:n.660_661insT
NM_000325.6:c.660_661insT MANE Select	NP_000316.2:n.660_661insT
NM_001204397.2:c.660_661insT	NP_001191326.1:n.660_661insT
NM_153426.3:c.660_661insT	NP_700475.1:n.660_661insT
NM_153427.3:c.660_661insT	NP_700476.1:n.660_661insT