Canonical Allele Identifier: CA449759853

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814881A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847104A>G , CM000668.2:g.32847104A>G	GRCh38
NC_000006.11:g.32814881A>G , CM000668.1:g.32814881A>G	GRCh37
NC_000006.10:g.32922859A>G	NCBI36
NG_011759.1:g.11868T>C
NG_028165.1:g.2832T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698420.1:c.*1156T>C (TAP1)	ENSP00000513708.1:n.*1156T>C
ENST00000698421.1:c.*898T>C (TAP1)	ENSP00000513709.1:n.*898T>C
ENST00000698422.1:c.1815T>C (TAP1)	ENSP00000513710.1:p.Asp605=
ENST00000698423.1:c.2004T>C (TAP1)	ENSP00000513711.1:p.Asp668=
ENST00000698424.1:c.1875T>C (TAP1)	ENSP00000513712.1:p.Asp625=
ENST00000354258.5:c.2004T>C (TAP1) MANE Select	ENSP00000346206.5:p.Asp668=
ENST00000643049.2:c.549T>C (TAP1)	ENSP00000494148.2:p.Asp183=
ENST00000643923.1:n.1440T>C (TAP1)
ENST00000645078.1:n.1599T>C (TAP1)
ENST00000354258.4:c.2184T>C (TAP1)	ENSP00000346206.4:p.Asp728=
ENST00000395330.5:c.-10+2830A>G (PSMB9)	ENSP00000378739.1:n.-10+2830A>G
ENST00000414474.5:c.-10+2234A>G (PSMB9)	ENSP00000394363.1:n.-10+2234A>G
ENST00000486332.1:n.1929T>C (TAP1)
ENST00000487296.1:n.884T>C (TAP1)
NM_000593.5:c.2184T>C (TAP1)	NP_000584.2:p.Asp728=
NM_001292022.1:c.1401T>C (TAP1)	NP_001278951.1:p.Asp467=
NM_001292022.2:c.1401T>C (TAP1)	NP_001278951.1:p.Asp467=
NM_000593.6:c.2004T>C (TAP1) MANE Select	NP_000584.3:p.Asp668=