Canonical Allele Identifier: CA363590371

Gene: TAP1 PSMB9 PSMB8-AS1

Linked Data

• MyVariant Identifiers: chr6:g.32813423T>G (hg19) ; chr6:g.32845646T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32845646T>G , CM000668.2:g.32845646T>G	GRCh38
NC_000006.11:g.32813423T>G , CM000668.1:g.32813423T>G	GRCh37
NC_000006.10:g.32921401T>G	NCBI36
NG_011759.1:g.13326A>C
NG_028165.1:g.4290A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1332A>C (TAP1)	ENSP00000513708.1:n.*1332A>C
ENST00000698421.1:c.*1074A>C (TAP1)	ENSP00000513709.1:n.*1074A>C
ENST00000698422.1:c.1991A>C (TAP1)	ENSP00000513710.1:p.Gln664Pro
ENST00000698423.1:c.2275A>C (TAP1)	ENSP00000513711.1:p.Ser759Arg
ENST00000698424.1:c.2051A>C (TAP1)	ENSP00000513712.1:p.Gln684Pro
ENST00000354258.5:c.2180A>C (TAP1) MANE Select	ENSP00000346206.5:p.Gln727Pro
ENST00000643049.2:c.725A>C (TAP1)	ENSP00000494148.2:p.Gln242Pro
ENST00000643923.1:n.1616A>C (TAP1)
ENST00000645078.1:n.1775A>C (TAP1)
ENST00000354258.4:c.2360A>C (TAP1)	ENSP00000346206.4:p.Gln787Pro
ENST00000395330.5:c.-10+1372T>G (PSMB9)	ENSP00000378739.1:n.-10+1372T>G
ENST00000414474.5:c.-10+776T>G (PSMB9)	ENSP00000394363.1:n.-10+776T>G
ENST00000486332.1:n.2105A>C (TAP1)
NM_000593.5:c.2360A>C (TAP1)	NP_000584.2:p.Gln787Pro
NM_001292022.1:c.1577A>C (TAP1)	NP_001278951.1:p.Gln526Pro
NR_037173.1:n.644T>G (PSMB8-AS1)
NR_037174.1:n.506T>G (PSMB8-AS1)
NR_037175.1:n.479T>G (PSMB8-AS1)
NR_037176.1:n.418T>G (PSMB8-AS1)
NM_001292022.2:c.1577A>C (TAP1)	NP_001278951.1:p.Gln526Pro
NM_000593.6:c.2180A>C (TAP1) MANE Select	NP_000584.3:p.Gln727Pro