Canonical Allele Identifier: CA449759928

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32814935T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847158T>A , CM000668.2:g.32847158T>A	GRCh38
NC_000006.11:g.32814935T>A , CM000668.1:g.32814935T>A	GRCh37
NC_000006.10:g.32922913T>A	NCBI36
NG_011759.1:g.11814A>T
NG_028165.1:g.2778A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1102A>T (TAP1)	ENSP00000513708.1:n.*1102A>T
ENST00000698421.1:c.*844A>T (TAP1)	ENSP00000513709.1:n.*844A>T
ENST00000698422.1:c.1761A>T (TAP1)	ENSP00000513710.1:p.Ala587=
ENST00000698423.1:c.1950A>T (TAP1)	ENSP00000513711.1:p.Ala650=
ENST00000698424.1:c.1821A>T (TAP1)	ENSP00000513712.1:p.Ala607=
ENST00000354258.5:c.1950A>T (TAP1) MANE Select	ENSP00000346206.5:p.Ala650=
ENST00000643049.2:c.495A>T (TAP1)	ENSP00000494148.2:p.Ala165=
ENST00000643923.1:n.1386A>T (TAP1)
ENST00000645078.1:n.1545A>T (TAP1)
ENST00000354258.4:c.2130A>T (TAP1)	ENSP00000346206.4:p.Ala710=
ENST00000395330.5:c.-10+2884T>A (PSMB9)	ENSP00000378739.1:n.-10+2884T>A
ENST00000414474.5:c.-10+2288T>A (PSMB9)	ENSP00000394363.1:n.-10+2288T>A
ENST00000486332.1:n.1875A>T (TAP1)
ENST00000487296.1:n.830A>T (TAP1)
NM_000593.5:c.2130A>T (TAP1)	NP_000584.2:p.Ala710=
NM_001292022.1:c.1347A>T (TAP1)	NP_001278951.1:p.Ala449=
NM_001292022.2:c.1347A>T (TAP1)	NP_001278951.1:p.Ala449=
NM_000593.6:c.1950A>T (TAP1) MANE Select	NP_000584.3:p.Ala650=