Canonical Allele Identifier: CA363590666

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814843A>C (hg19) ; chr6:g.32847066A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847066A>C , CM000668.2:g.32847066A>C	GRCh38
NC_000006.11:g.32814843A>C , CM000668.1:g.32814843A>C	GRCh37
NC_000006.10:g.32922821A>C	NCBI36
NG_011759.1:g.11906T>G
NG_028165.1:g.2870T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1192+2T>G (TAP1)	ENSP00000513708.1:n.*1192+2T>G
ENST00000698421.1:c.*934+2T>G (TAP1)	ENSP00000513709.1:n.*934+2T>G
ENST00000698422.1:c.1851+2T>G (TAP1)	ENSP00000513710.1:n.1851+2T>G
ENST00000698423.1:c.2040+2T>G (TAP1)	ENSP00000513711.1:n.2040+2T>G
ENST00000698424.1:c.1911+2T>G (TAP1)	ENSP00000513712.1:n.1911+2T>G
ENST00000354258.5:c.2040+2T>G (TAP1) MANE Select	ENSP00000346206.5:n.2040+2T>G
ENST00000643049.2:c.585+2T>G (TAP1)	ENSP00000494148.2:n.585+2T>G
ENST00000643923.1:n.1476+2T>G (TAP1)
ENST00000645078.1:n.1635+2T>G (TAP1)
ENST00000354258.4:c.2220+2T>G (TAP1)	ENSP00000346206.4:n.2220+2T>G
ENST00000395330.5:c.-10+2792A>C (PSMB9)	ENSP00000378739.1:n.-10+2792A>C
ENST00000414474.5:c.-10+2196A>C (PSMB9)	ENSP00000394363.1:n.-10+2196A>C
ENST00000486332.1:n.1965+2T>G (TAP1)
ENST00000487296.1:n.920+2T>G (TAP1)
NM_000593.5:c.2220+2T>G (TAP1)	NP_000584.2:n.2220+2T>G
NM_001292022.1:c.1437+2T>G (TAP1)	NP_001278951.1:n.1437+2T>G
NM_001292022.2:c.1437+2T>G (TAP1)	NP_001278951.1:n.1437+2T>G
NM_000593.6:c.2040+2T>G (TAP1) MANE Select	NP_000584.3:n.2040+2T>G