Canonical Allele Identifier: CA363590708

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814859T>C (hg19) ; chr6:g.32847082T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847082T>C , CM000668.2:g.32847082T>C	GRCh38
NC_000006.11:g.32814859T>C , CM000668.1:g.32814859T>C	GRCh37
NC_000006.10:g.32922837T>C	NCBI36
NG_011759.1:g.11890A>G
NG_028165.1:g.2854A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1178A>G (TAP1)	ENSP00000513708.1:n.*1178A>G
ENST00000698421.1:c.*920A>G (TAP1)	ENSP00000513709.1:n.*920A>G
ENST00000698422.1:c.1837A>G (TAP1)	ENSP00000513710.1:p.Asn613Asp
ENST00000698423.1:c.2026A>G (TAP1)	ENSP00000513711.1:p.Asn676Asp
ENST00000698424.1:c.1897A>G (TAP1)	ENSP00000513712.1:p.Asn633Asp
ENST00000354258.5:c.2026A>G (TAP1) MANE Select	ENSP00000346206.5:p.Asn676Asp
ENST00000643049.2:c.571A>G (TAP1)	ENSP00000494148.2:p.Asn191Asp
ENST00000643923.1:n.1462A>G (TAP1)
ENST00000645078.1:n.1621A>G (TAP1)
ENST00000354258.4:c.2206A>G (TAP1)	ENSP00000346206.4:p.Asn736Asp
ENST00000395330.5:c.-10+2808T>C (PSMB9)	ENSP00000378739.1:n.-10+2808T>C
ENST00000414474.5:c.-10+2212T>C (PSMB9)	ENSP00000394363.1:n.-10+2212T>C
ENST00000486332.1:n.1951A>G (TAP1)
ENST00000487296.1:n.906A>G (TAP1)
NM_000593.5:c.2206A>G (TAP1)	NP_000584.2:p.Asn736Asp
NM_001292022.1:c.1423A>G (TAP1)	NP_001278951.1:p.Asn475Asp
NM_001292022.2:c.1423A>G (TAP1)	NP_001278951.1:p.Asn475Asp
NM_000593.6:c.2026A>G (TAP1) MANE Select	NP_000584.3:p.Asn676Asp