Canonical Allele Identifier: CA1619762302

Gene: TAP1 PSMB9

Linked Data

• dbSNP Id: rs1770469711

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847082_32847087del , CM000668.2:g.32847082_32847087del	GRCh38
NC_000006.11:g.32814859_32814864del , CM000668.1:g.32814859_32814864del	GRCh37
NC_000006.10:g.32922837_32922842del	NCBI36
NG_011759.1:g.11886_11891del
NG_028165.1:g.2850_2855del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1174_*1179del (TAP1)	ENSP00000513708.1:n.*1174_*1179del
ENST00000698421.1:c.*916_*921del (TAP1)	ENSP00000513709.1:n.*916_*921del
ENST00000698422.1:c.1833_1838del (TAP1)	ENSP00000513710.1:p.Ala612_Asn613del
ENST00000698423.1:c.2022_2027del (TAP1)	ENSP00000513711.1:p.Ala675_Asn676del
ENST00000698424.1:c.1893_1898del (TAP1)	ENSP00000513712.1:p.Ala632_Asn633del
ENST00000354258.5:c.2022_2027del (TAP1) MANE Select	ENSP00000346206.5:p.Ala675_Asn676del
ENST00000643049.2:c.567_572del (TAP1)	ENSP00000494148.2:p.Ala190_Asn191del
ENST00000643923.1:n.1458_1463del (TAP1)
ENST00000645078.1:n.1617_1622del (TAP1)
ENST00000354258.4:c.2202_2207del (TAP1)	ENSP00000346206.4:p.Ala735_Asn736del
ENST00000395330.5:c.-10+2808_-10+2813del (PSMB9)	ENSP00000378739.1:n.-10+2808_-10+2813del
ENST00000414474.5:c.-10+2212_-10+2217del (PSMB9)	ENSP00000394363.1:n.-10+2212_-10+2217del
ENST00000486332.1:n.1947_1952del (TAP1)
ENST00000487296.1:n.902_907del (TAP1)
NM_000593.5:c.2202_2207del (TAP1)	NP_000584.2:p.Ala735_Asn736del
NM_001292022.1:c.1419_1424del (TAP1)	NP_001278951.1:p.Ala474_Asn475del
NM_001292022.2:c.1419_1424del (TAP1)	NP_001278951.1:p.Ala474_Asn475del
NM_000593.6:c.2022_2027del (TAP1) MANE Select	NP_000584.3:p.Ala675_Asn676del