Canonical Allele Identifier: CA363590767

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814888A>C (hg19) ; chr6:g.32847111A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847111A>C , CM000668.2:g.32847111A>C	GRCh38
NC_000006.11:g.32814888A>C , CM000668.1:g.32814888A>C	GRCh37
NC_000006.10:g.32922866A>C	NCBI36
NG_011759.1:g.11861T>G
NG_028165.1:g.2825T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1149T>G (TAP1)	ENSP00000513708.1:n.*1149T>G
ENST00000698421.1:c.*891T>G (TAP1)	ENSP00000513709.1:n.*891T>G
ENST00000698422.1:c.1808T>G (TAP1)	ENSP00000513710.1:p.Leu603Arg
ENST00000698423.1:c.1997T>G (TAP1)	ENSP00000513711.1:p.Leu666Arg
ENST00000698424.1:c.1868T>G (TAP1)	ENSP00000513712.1:p.Leu623Arg
ENST00000354258.5:c.1997T>G (TAP1) MANE Select	ENSP00000346206.5:p.Leu666Arg
ENST00000643049.2:c.542T>G (TAP1)	ENSP00000494148.2:p.Leu181Arg
ENST00000643923.1:n.1433T>G (TAP1)
ENST00000645078.1:n.1592T>G (TAP1)
ENST00000354258.4:c.2177T>G (TAP1)	ENSP00000346206.4:p.Leu726Arg
ENST00000395330.5:c.-10+2837A>C (PSMB9)	ENSP00000378739.1:n.-10+2837A>C
ENST00000414474.5:c.-10+2241A>C (PSMB9)	ENSP00000394363.1:n.-10+2241A>C
ENST00000486332.1:n.1922T>G (TAP1)
ENST00000487296.1:n.877T>G (TAP1)
NM_000593.5:c.2177T>G (TAP1)	NP_000584.2:p.Leu726Arg
NM_001292022.1:c.1394T>G (TAP1)	NP_001278951.1:p.Leu465Arg
NM_001292022.2:c.1394T>G (TAP1)	NP_001278951.1:p.Leu465Arg
NM_000593.6:c.1997T>G (TAP1) MANE Select	NP_000584.3:p.Leu666Arg