Canonical Allele Identifier: CA363590947

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814978A>C (hg19) ; chr6:g.32847201A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847201A>C , CM000668.2:g.32847201A>C	GRCh38
NC_000006.11:g.32814978A>C , CM000668.1:g.32814978A>C	GRCh37
NC_000006.10:g.32922956A>C	NCBI36
NG_011759.1:g.11771T>G
NG_028165.1:g.2735T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1059T>G (TAP1)	ENSP00000513708.1:n.*1059T>G
ENST00000698421.1:c.*801T>G (TAP1)	ENSP00000513709.1:n.*801T>G
ENST00000698422.1:c.1718T>G (TAP1)	ENSP00000513710.1:p.Val573Gly
ENST00000698423.1:c.1907T>G (TAP1)	ENSP00000513711.1:p.Val636Gly
ENST00000698424.1:c.1778T>G (TAP1)	ENSP00000513712.1:p.Val593Gly
ENST00000354258.5:c.1907T>G (TAP1) MANE Select	ENSP00000346206.5:p.Val636Gly
ENST00000643049.2:c.452T>G (TAP1)	ENSP00000494148.2:p.Val151Gly
ENST00000643923.1:n.1343T>G (TAP1)
ENST00000645078.1:n.1502T>G (TAP1)
ENST00000354258.4:c.2087T>G (TAP1)	ENSP00000346206.4:p.Val696Gly
ENST00000395330.5:c.-10+2927A>C (PSMB9)	ENSP00000378739.1:n.-10+2927A>C
ENST00000414474.5:c.-10+2331A>C (PSMB9)	ENSP00000394363.1:n.-10+2331A>C
ENST00000486332.1:n.1832T>G (TAP1)
ENST00000487296.1:n.787T>G (TAP1)
NM_000593.5:c.2087T>G (TAP1)	NP_000584.2:p.Val696Gly
NM_001292022.1:c.1304T>G (TAP1)	NP_001278951.1:p.Val435Gly
NM_001292022.2:c.1304T>G (TAP1)	NP_001278951.1:p.Val435Gly
NM_000593.6:c.1907T>G (TAP1) MANE Select	NP_000584.3:p.Val636Gly