Canonical Allele Identifier: CA449759823

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814863A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847086A>G , CM000668.2:g.32847086A>G	GRCh38
NC_000006.11:g.32814863A>G , CM000668.1:g.32814863A>G	GRCh37
NC_000006.10:g.32922841A>G	NCBI36
NG_011759.1:g.11886T>C
NG_028165.1:g.2850T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1174T>C (TAP1)	ENSP00000513708.1:n.*1174T>C
ENST00000698421.1:c.*916T>C (TAP1)	ENSP00000513709.1:n.*916T>C
ENST00000698422.1:c.1833T>C (TAP1)	ENSP00000513710.1:p.Asp611=
ENST00000698423.1:c.2022T>C (TAP1)	ENSP00000513711.1:p.Asp674=
ENST00000698424.1:c.1893T>C (TAP1)	ENSP00000513712.1:p.Asp631=
ENST00000354258.5:c.2022T>C (TAP1) MANE Select	ENSP00000346206.5:p.Asp674=
ENST00000643049.2:c.567T>C (TAP1)	ENSP00000494148.2:p.Asp189=
ENST00000643923.1:n.1458T>C (TAP1)
ENST00000645078.1:n.1617T>C (TAP1)
ENST00000354258.4:c.2202T>C (TAP1)	ENSP00000346206.4:p.Asp734=
ENST00000395330.5:c.-10+2812A>G (PSMB9)	ENSP00000378739.1:n.-10+2812A>G
ENST00000414474.5:c.-10+2216A>G (PSMB9)	ENSP00000394363.1:n.-10+2216A>G
ENST00000486332.1:n.1947T>C (TAP1)
ENST00000487296.1:n.902T>C (TAP1)
NM_000593.5:c.2202T>C (TAP1)	NP_000584.2:p.Asp734=
NM_001292022.1:c.1419T>C (TAP1)	NP_001278951.1:p.Asp473=
NM_001292022.2:c.1419T>C (TAP1)	NP_001278951.1:p.Asp473=
NM_000593.6:c.2022T>C (TAP1) MANE Select	NP_000584.3:p.Asp674=