Canonical Allele Identifier: CA2678187192

Gene: TAP1 PSMB9

Linked Data

• gnomAD v4: 6-32850910-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32850910G>T , CM000668.2:g.32850910G>T	GRCh38
NC_000006.11:g.32818687G>T , CM000668.1:g.32818687G>T	GRCh37
NC_000006.10:g.32926665G>T	NCBI36
NG_011759.1:g.8062C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*202+34C>A (TAP1)	ENSP00000513708.1:n.*202+34C>A
ENST00000698421.1:c.845-393C>A (TAP1)	ENSP00000513709.1:n.845-393C>A
ENST00000698422.1:c.1050+34C>A (TAP1)	ENSP00000513710.1:n.1050+34C>A
ENST00000698423.1:c.1050+34C>A (TAP1)	ENSP00000513711.1:n.1050+34C>A
ENST00000698424.1:c.1050+34C>A (TAP1)	ENSP00000513712.1:n.1050+34C>A
ENST00000354258.5:c.1050+34C>A (TAP1) MANE Select	ENSP00000346206.5:n.1050+34C>A
ENST00000643049.2:c.141+2586C>A (TAP1)	ENSP00000494148.2:n.141+2586C>A
ENST00000643923.1:n.486+34C>A (TAP1)
ENST00000645078.1:n.645+34C>A (TAP1)
ENST00000354258.4:c.1230+34C>A (TAP1)	ENSP00000346206.4:n.1230+34C>A
ENST00000395330.5:c.-9-5228G>T (PSMB9)	ENSP00000378739.1:n.-9-5228G>T
ENST00000414474.5:c.-9-5228G>T (PSMB9)	ENSP00000394363.1:n.-9-5228G>T
NM_000593.5:c.1230+34C>A (TAP1)	NP_000584.2:n.1230+34C>A
NM_001292022.1:c.447+34C>A (TAP1)	NP_001278951.1:n.447+34C>A
NM_001292022.2:c.447+34C>A (TAP1)	NP_001278951.1:n.447+34C>A
NM_000593.6:c.1050+34C>A (TAP1) MANE Select	NP_000584.3:n.1050+34C>A