Canonical Allele Identifier: CA363590769

Gene: TAP1 PSMB9

Linked Data

• gnomAD v4: 6-32847111-A-T
• MyVariant Identifiers: chr6:g.32814888A>T (hg19) ; chr6:g.32847111A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847111A>T , CM000668.2:g.32847111A>T	GRCh38
NC_000006.11:g.32814888A>T , CM000668.1:g.32814888A>T	GRCh37
NC_000006.10:g.32922866A>T	NCBI36
NG_011759.1:g.11861T>A
NG_028165.1:g.2825T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1149T>A (TAP1)	ENSP00000513708.1:n.*1149T>A
ENST00000698421.1:c.*891T>A (TAP1)	ENSP00000513709.1:n.*891T>A
ENST00000698422.1:c.1808T>A (TAP1)	ENSP00000513710.1:p.Leu603Gln
ENST00000698423.1:c.1997T>A (TAP1)	ENSP00000513711.1:p.Leu666Gln
ENST00000698424.1:c.1868T>A (TAP1)	ENSP00000513712.1:p.Leu623Gln
ENST00000354258.5:c.1997T>A (TAP1) MANE Select	ENSP00000346206.5:p.Leu666Gln
ENST00000643049.2:c.542T>A (TAP1)	ENSP00000494148.2:p.Leu181Gln
ENST00000643923.1:n.1433T>A (TAP1)
ENST00000645078.1:n.1592T>A (TAP1)
ENST00000354258.4:c.2177T>A (TAP1)	ENSP00000346206.4:p.Leu726Gln
ENST00000395330.5:c.-10+2837A>T (PSMB9)	ENSP00000378739.1:n.-10+2837A>T
ENST00000414474.5:c.-10+2241A>T (PSMB9)	ENSP00000394363.1:n.-10+2241A>T
ENST00000486332.1:n.1922T>A (TAP1)
ENST00000487296.1:n.877T>A (TAP1)
NM_000593.5:c.2177T>A (TAP1)	NP_000584.2:p.Leu726Gln
NM_001292022.1:c.1394T>A (TAP1)	NP_001278951.1:p.Leu465Gln
NM_001292022.2:c.1394T>A (TAP1)	NP_001278951.1:p.Leu465Gln
NM_000593.6:c.1997T>A (TAP1) MANE Select	NP_000584.3:p.Leu666Gln