Canonical Allele Identifier: CA363592872

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32818731T>G (hg19) ; chr6:g.32850954T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32850954T>G , CM000668.2:g.32850954T>G	GRCh38
NC_000006.11:g.32818731T>G , CM000668.1:g.32818731T>G	GRCh37
NC_000006.10:g.32926709T>G	NCBI36
NG_011759.1:g.8018A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*192A>C (TAP1)	ENSP00000513708.1:n.*192A>C
ENST00000698421.1:c.845-437A>C (TAP1)	ENSP00000513709.1:n.845-437A>C
ENST00000698422.1:c.1040A>C (TAP1)	ENSP00000513710.1:p.Lys347Thr
ENST00000698423.1:c.1040A>C (TAP1)	ENSP00000513711.1:p.Lys347Thr
ENST00000698424.1:c.1040A>C (TAP1)	ENSP00000513712.1:p.Lys347Thr
ENST00000354258.5:c.1040A>C (TAP1) MANE Select	ENSP00000346206.5:p.Lys347Thr
ENST00000643049.2:c.141+2542A>C (TAP1)	ENSP00000494148.2:n.141+2542A>C
ENST00000643923.1:n.476A>C (TAP1)
ENST00000645078.1:n.635A>C (TAP1)
ENST00000354258.4:c.1220A>C (TAP1)	ENSP00000346206.4:p.Lys407Thr
ENST00000395330.5:c.-9-5184T>G (PSMB9)	ENSP00000378739.1:n.-9-5184T>G
ENST00000414474.5:c.-9-5184T>G (PSMB9)	ENSP00000394363.1:n.-9-5184T>G
NM_000593.5:c.1220A>C (TAP1)	NP_000584.2:p.Lys407Thr
NM_001292022.1:c.437A>C (TAP1)	NP_001278951.1:p.Lys146Thr
NM_001292022.2:c.437A>C (TAP1)	NP_001278951.1:p.Lys146Thr
NM_000593.6:c.1040A>C (TAP1) MANE Select	NP_000584.3:p.Lys347Thr