Canonical Allele Identifier: CA363590760

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814884A>C (hg19) ; chr6:g.32847107A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847107A>C , CM000668.2:g.32847107A>C	GRCh38
NC_000006.11:g.32814884A>C , CM000668.1:g.32814884A>C	GRCh37
NC_000006.10:g.32922862A>C	NCBI36
NG_011759.1:g.11865T>G
NG_028165.1:g.2829T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1153T>G (TAP1)	ENSP00000513708.1:n.*1153T>G
ENST00000698421.1:c.*895T>G (TAP1)	ENSP00000513709.1:n.*895T>G
ENST00000698422.1:c.1812T>G (TAP1)	ENSP00000513710.1:p.Asp604Glu
ENST00000698423.1:c.2001T>G (TAP1)	ENSP00000513711.1:p.Asp667Glu
ENST00000698424.1:c.1872T>G (TAP1)	ENSP00000513712.1:p.Asp624Glu
ENST00000354258.5:c.2001T>G (TAP1) MANE Select	ENSP00000346206.5:p.Asp667Glu
ENST00000643049.2:c.546T>G (TAP1)	ENSP00000494148.2:p.Asp182Glu
ENST00000643923.1:n.1437T>G (TAP1)
ENST00000645078.1:n.1596T>G (TAP1)
ENST00000354258.4:c.2181T>G (TAP1)	ENSP00000346206.4:p.Asp727Glu
ENST00000395330.5:c.-10+2833A>C (PSMB9)	ENSP00000378739.1:n.-10+2833A>C
ENST00000414474.5:c.-10+2237A>C (PSMB9)	ENSP00000394363.1:n.-10+2237A>C
ENST00000486332.1:n.1926T>G (TAP1)
ENST00000487296.1:n.881T>G (TAP1)
NM_000593.5:c.2181T>G (TAP1)	NP_000584.2:p.Asp727Glu
NM_001292022.1:c.1398T>G (TAP1)	NP_001278951.1:p.Asp466Glu
NM_001292022.2:c.1398T>G (TAP1)	NP_001278951.1:p.Asp466Glu
NM_000593.6:c.2001T>G (TAP1) MANE Select	NP_000584.3:p.Asp667Glu