Canonical Allele Identifier: CA449760998

Gene: TAP1 PSMB9

Linked Data

• MyVariant Identifiers: chr6:g.32818730T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32850953T>C , CM000668.2:g.32850953T>C	GRCh38
NC_000006.11:g.32818730T>C , CM000668.1:g.32818730T>C	GRCh37
NC_000006.10:g.32926708T>C	NCBI36
NG_011759.1:g.8019A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*193A>G (TAP1)	ENSP00000513708.1:n.*193A>G
ENST00000698421.1:c.845-436A>G (TAP1)	ENSP00000513709.1:n.845-436A>G
ENST00000698422.1:c.1041A>G (TAP1)	ENSP00000513710.1:p.Lys347=
ENST00000698423.1:c.1041A>G (TAP1)	ENSP00000513711.1:p.Lys347=
ENST00000698424.1:c.1041A>G (TAP1)	ENSP00000513712.1:p.Lys347=
ENST00000354258.5:c.1041A>G (TAP1) MANE Select	ENSP00000346206.5:p.Lys347=
ENST00000643049.2:c.141+2543A>G (TAP1)	ENSP00000494148.2:n.141+2543A>G
ENST00000643923.1:n.477A>G (TAP1)
ENST00000645078.1:n.636A>G (TAP1)
ENST00000354258.4:c.1221A>G (TAP1)	ENSP00000346206.4:p.Lys407=
ENST00000395330.5:c.-9-5185T>C (PSMB9)	ENSP00000378739.1:n.-9-5185T>C
ENST00000414474.5:c.-9-5185T>C (PSMB9)	ENSP00000394363.1:n.-9-5185T>C
NM_000593.5:c.1221A>G (TAP1)	NP_000584.2:p.Lys407=
NM_001292022.1:c.438A>G (TAP1)	NP_001278951.1:p.Lys146=
NM_001292022.2:c.438A>G (TAP1)	NP_001278951.1:p.Lys146=
NM_000593.6:c.1041A>G (TAP1) MANE Select	NP_000584.3:p.Lys347=