Canonical Allele Identifier: CA2578579732

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847263_32847264insACACACA , CM000668.2:g.32847263_32847264insACACACA	GRCh38
NC_000006.11:g.32815040_32815041insACACACA , CM000668.1:g.32815040_32815041insACACACA	GRCh37
NC_000006.10:g.32923018_32923019insACACACA	NCBI36
NG_011759.1:g.11708_11709insTGTGTGT
NG_028165.1:g.2672_2673insTGTGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1056-60_*1056-59insTGTGTGT (TAP1)	ENSP00000513708.1:n.*1056-60_*1056-59insTGTGTGT
ENST00000698421.1:c.*798-60_*798-59insTGTGTGT (TAP1)	ENSP00000513709.1:n.*798-60_*798-59insTGTGTGT
ENST00000698422.1:c.1715-60_1715-59insTGTGTGT (TAP1)	ENSP00000513710.1:n.1715-60_1715-59insTGTGTGT
ENST00000698423.1:c.1904-60_1904-59insTGTGTGT (TAP1)	ENSP00000513711.1:n.1904-60_1904-59insTGTGTGT
ENST00000698424.1:c.1775-60_1775-59insTGTGTGT (TAP1)	ENSP00000513712.1:n.1775-60_1775-59insTGTGTGT
ENST00000354258.5:c.1904-60_1904-59insTGTGTGT (TAP1) MANE Select	ENSP00000346206.5:n.1904-60_1904-59insTGTGTGT
ENST00000643049.2:c.449-60_449-59insTGTGTGT (TAP1)	ENSP00000494148.2:n.449-60_449-59insTGTGTGT
ENST00000643923.1:n.1340-60_1340-59insTGTGTGT (TAP1)
ENST00000645078.1:n.1499-60_1499-59insTGTGTGT (TAP1)
ENST00000354258.4:c.2084-60_2084-59insTGTGTGT (TAP1)	ENSP00000346206.4:n.2084-60_2084-59insTGTGTGT
ENST00000395330.5:c.-10+2989_-10+2990insACACACA (PSMB9)	ENSP00000378739.1:n.-10+2989_-10+2990insACACACA
ENST00000414474.5:c.-10+2393_-10+2394insACACACA (PSMB9)	ENSP00000394363.1:n.-10+2393_-10+2394insACACACA
ENST00000486332.1:n.1829-60_1829-59insTGTGTGT (TAP1)
ENST00000487296.1:n.724_725insTGTGTGT (TAP1)
NM_000593.5:c.2084-60_2084-59insTGTGTGT (TAP1)	NP_000584.2:n.2084-60_2084-59insTGTGTGT
NM_001292022.1:c.1301-60_1301-59insTGTGTGT (TAP1)	NP_001278951.1:n.1301-60_1301-59insTGTGTGT
NM_001292022.2:c.1301-60_1301-59insTGTGTGT (TAP1)	NP_001278951.1:n.1301-60_1301-59insTGTGTGT
NM_000593.6:c.1904-60_1904-59insTGTGTGT (TAP1) MANE Select	NP_000584.3:n.1904-60_1904-59insTGTGTGT