Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19943671_19943672delinsAT , CM000684.2:g.19943671_19943672delinsAT	GRCh38
NC_000022.10:g.19931194_19931195delinsAT , CM000684.1:g.19931194_19931195delinsAT	GRCh37
NC_000022.9:g.18311194_18311195delinsAT	NCBI36
NG_011526.1:g.6932_6933delinsAT
NG_011835.1:g.3165_3166delinsAT , LRG_417:g.3165_3166delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361682.11:c.-92+1774_-92+1775delinsAT MANE Select	ENSP00000354511.6:n.-92+1774_-92+1775delinsAT
ENST00000428707.2:c.-92+1774_-92+1775delinsAT	ENSP00000387695.2:n.-92+1774_-92+1775delinsAT
ENST00000676678.1:c.-92+2096_-92+2097delinsAT	ENSP00000503719.1:n.-92+2096_-92+2097delinsAT
ENST00000678769.1:c.-92+1774_-92+1775delinsAT	ENSP00000503289.1:n.-92+1774_-92+1775delinsAT
ENST00000678868.1:c.-276+1774_-276+1775delinsAT	ENSP00000503583.1:n.-276+1774_-276+1775delinsAT
ENST00000361682.10:c.-92+1774_-92+1775delinsAT	ENSP00000354511.6:n.-92+1774_-92+1775delinsAT
ENST00000403184.5:c.-92+1774_-92+1775delinsAT	ENSP00000383966.1:n.-92+1774_-92+1775delinsAT
ENST00000403710.5:c.-386+1774_-386+1775delinsAT	ENSP00000385917.1:n.-386+1774_-386+1775delinsAT
ENST00000407537.5:c.-270+1774_-270+1775delinsAT	ENSP00000384654.2:n.-270+1774_-270+1775delinsAT
ENST00000467943.5:n.105+1774_105+1775delinsAT
NM_000754.3:c.-92+1774_-92+1775delinsAT	NP_000745.1:n.-92+1774_-92+1775delinsAT
XM_011529887.1:c.-92+1774_-92+1775delinsAT	XP_011528189.1:n.-92+1774_-92+1775delinsAT
XM_011529890.1:c.-386+1774_-386+1775delinsAT	XP_011528192.1:n.-386+1774_-386+1775delinsAT
XM_011529891.1:c.-386+1496_-386+1497delinsAT	XP_011528193.1:n.-386+1496_-386+1497delinsAT
NM_001362828.1:c.-386+1774_-386+1775delinsAT	NP_001349757.1:n.-386+1774_-386+1775delinsAT
XM_017028595.1:c.-386+1496_-386+1497delinsAT	XP_016884084.1:n.-386+1496_-386+1497delinsAT
NM_000754.4:c.-92+1774_-92+1775delinsAT MANE Select	NP_000745.1:n.-92+1774_-92+1775delinsAT
NM_001362828.2:c.-386+1774_-386+1775delinsAT	NP_001349757.1:n.-386+1774_-386+1775delinsAT