Canonical Allele Identifier: CA363590676

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814846T>G (hg19) ; chr6:g.32847069T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847069T>G , CM000668.2:g.32847069T>G	GRCh38
NC_000006.11:g.32814846T>G , CM000668.1:g.32814846T>G	GRCh37
NC_000006.10:g.32922824T>G	NCBI36
NG_011759.1:g.11903A>C
NG_028165.1:g.2867A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1191A>C (TAP1)	ENSP00000513708.1:n.*1191A>C
ENST00000698421.1:c.*933A>C (TAP1)	ENSP00000513709.1:n.*933A>C
ENST00000698422.1:c.1850A>C (TAP1)	ENSP00000513710.1:p.Gln617Pro
ENST00000698423.1:c.2039A>C (TAP1)	ENSP00000513711.1:p.Gln680Pro
ENST00000698424.1:c.1910A>C (TAP1)	ENSP00000513712.1:p.Gln637Pro
ENST00000354258.5:c.2039A>C (TAP1) MANE Select	ENSP00000346206.5:p.Gln680Pro
ENST00000643049.2:c.584A>C (TAP1)	ENSP00000494148.2:p.Gln195Pro
ENST00000643923.1:n.1475A>C (TAP1)
ENST00000645078.1:n.1634A>C (TAP1)
ENST00000354258.4:c.2219A>C (TAP1)	ENSP00000346206.4:p.Gln740Pro
ENST00000395330.5:c.-10+2795T>G (PSMB9)	ENSP00000378739.1:n.-10+2795T>G
ENST00000414474.5:c.-10+2199T>G (PSMB9)	ENSP00000394363.1:n.-10+2199T>G
ENST00000486332.1:n.1964A>C (TAP1)
ENST00000487296.1:n.919A>C (TAP1)
NM_000593.5:c.2219A>C (TAP1)	NP_000584.2:p.Gln740Pro
NM_001292022.1:c.1436A>C (TAP1)	NP_001278951.1:p.Gln479Pro
NM_001292022.2:c.1436A>C (TAP1)	NP_001278951.1:p.Gln479Pro
NM_000593.6:c.2039A>C (TAP1) MANE Select	NP_000584.3:p.Gln680Pro