Canonical Allele Identifier: CA363590730

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814871C>T (hg19) ; chr6:g.32847094C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847094C>T , CM000668.2:g.32847094C>T	GRCh38
NC_000006.11:g.32814871C>T , CM000668.1:g.32814871C>T	GRCh37
NC_000006.10:g.32922849C>T	NCBI36
NG_011759.1:g.11878G>A
NG_028165.1:g.2842G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1166G>A (TAP1)	ENSP00000513708.1:n.*1166G>A
ENST00000698421.1:c.*908G>A (TAP1)	ENSP00000513709.1:n.*908G>A
ENST00000698422.1:c.1825G>A (TAP1)	ENSP00000513710.1:p.Ala609Thr
ENST00000698423.1:c.2014G>A (TAP1)	ENSP00000513711.1:p.Ala672Thr
ENST00000698424.1:c.1885G>A (TAP1)	ENSP00000513712.1:p.Ala629Thr
ENST00000354258.5:c.2014G>A (TAP1) MANE Select	ENSP00000346206.5:p.Ala672Thr
ENST00000643049.2:c.559G>A (TAP1)	ENSP00000494148.2:p.Ala187Thr
ENST00000643923.1:n.1450G>A (TAP1)
ENST00000645078.1:n.1609G>A (TAP1)
ENST00000354258.4:c.2194G>A (TAP1)	ENSP00000346206.4:p.Ala732Thr
ENST00000395330.5:c.-10+2820C>T (PSMB9)	ENSP00000378739.1:n.-10+2820C>T
ENST00000414474.5:c.-10+2224C>T (PSMB9)	ENSP00000394363.1:n.-10+2224C>T
ENST00000486332.1:n.1939G>A (TAP1)
ENST00000487296.1:n.894G>A (TAP1)
NM_000593.5:c.2194G>A (TAP1)	NP_000584.2:p.Ala732Thr
NM_001292022.1:c.1411G>A (TAP1)	NP_001278951.1:p.Ala471Thr
NM_001292022.2:c.1411G>A (TAP1)	NP_001278951.1:p.Ala471Thr
NM_000593.6:c.2014G>A (TAP1) MANE Select	NP_000584.3:p.Ala672Thr