Canonical Allele Identifier: CA363590884

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814946G>C (hg19) ; chr6:g.32847169G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847169G>C , CM000668.2:g.32847169G>C	GRCh38
NC_000006.11:g.32814946G>C , CM000668.1:g.32814946G>C	GRCh37
NC_000006.10:g.32922924G>C	NCBI36
NG_011759.1:g.11803C>G
NG_028165.1:g.2767C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1091C>G (TAP1)	ENSP00000513708.1:n.*1091C>G
ENST00000698421.1:c.*833C>G (TAP1)	ENSP00000513709.1:n.*833C>G
ENST00000698422.1:c.1750C>G (TAP1)	ENSP00000513710.1:p.Gln584Glu
ENST00000698423.1:c.1939C>G (TAP1)	ENSP00000513711.1:p.Gln647Glu
ENST00000698424.1:c.1810C>G (TAP1)	ENSP00000513712.1:p.Gln604Glu
ENST00000354258.5:c.1939C>G (TAP1) MANE Select	ENSP00000346206.5:p.Gln647Glu
ENST00000643049.2:c.484C>G (TAP1)	ENSP00000494148.2:p.Gln162Glu
ENST00000643923.1:n.1375C>G (TAP1)
ENST00000645078.1:n.1534C>G (TAP1)
ENST00000354258.4:c.2119C>G (TAP1)	ENSP00000346206.4:p.Gln707Glu
ENST00000395330.5:c.-10+2895G>C (PSMB9)	ENSP00000378739.1:n.-10+2895G>C
ENST00000414474.5:c.-10+2299G>C (PSMB9)	ENSP00000394363.1:n.-10+2299G>C
ENST00000486332.1:n.1864C>G (TAP1)
ENST00000487296.1:n.819C>G (TAP1)
NM_000593.5:c.2119C>G (TAP1)	NP_000584.2:p.Gln707Glu
NM_001292022.1:c.1336C>G (TAP1)	NP_001278951.1:p.Gln446Glu
NM_001292022.2:c.1336C>G (TAP1)	NP_001278951.1:p.Gln446Glu
NM_000593.6:c.1939C>G (TAP1) MANE Select	NP_000584.3:p.Gln647Glu