Canonical Allele Identifier: CA1619762267

Gene: TAP1 PSMB9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32847017_32847020delinsAAAG , CM000668.2:g.32847017_32847020delinsAAAG	GRCh38
NC_000006.11:g.32814794_32814797delinsAAAG , CM000668.1:g.32814794_32814797delinsAAAG	GRCh37
NC_000006.10:g.32922772_32922775delinsAAAG	NCBI36
NG_011759.1:g.11952_11955delinsCTTT
NG_028165.1:g.2916_2919delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698420.1:c.*1192+48_*1192+51delinsCTTT (TAP1)	ENSP00000513708.1:n.*1192+48_*1192+51delinsCTTT
ENST00000698421.1:c.*934+48_*934+51delinsCTTT (TAP1)	ENSP00000513709.1:n.*934+48_*934+51delinsCTTT
ENST00000698422.1:c.1851+48_1851+51delinsCTTT (TAP1)	ENSP00000513710.1:n.1851+48_1851+51delinsCTTT
ENST00000698423.1:c.2040+48_2040+51delinsCTTT (TAP1)	ENSP00000513711.1:n.2040+48_2040+51delinsCTTT
ENST00000698424.1:c.1911+48_1911+51delinsCTTT (TAP1)	ENSP00000513712.1:n.1911+48_1911+51delinsCTTT
ENST00000354258.5:c.2040+48_2040+51delinsCTTT (TAP1) MANE Select	ENSP00000346206.5:n.2040+48_2040+51delinsCTTT
ENST00000643049.2:c.585+48_585+51delinsCTTT (TAP1)	ENSP00000494148.2:n.585+48_585+51delinsCTTT
ENST00000643923.1:n.1476+48_1476+51delinsCTTT (TAP1)
ENST00000645078.1:n.1635+48_1635+51delinsCTTT (TAP1)
ENST00000354258.4:c.2220+48_2220+51delinsCTTT (TAP1)	ENSP00000346206.4:n.2220+48_2220+51delinsCTTT
ENST00000395330.5:c.-10+2743_-10+2746delinsAAAG (PSMB9)	ENSP00000378739.1:n.-10+2743_-10+2746delinsAAAG
ENST00000414474.5:c.-10+2147_-10+2150delinsAAAG (PSMB9)	ENSP00000394363.1:n.-10+2147_-10+2150delinsAAAG
ENST00000486332.1:n.1965+48_1965+51delinsCTTT (TAP1)
ENST00000487296.1:n.920+48_920+51delinsCTTT (TAP1)
NM_000593.5:c.2220+48_2220+51delinsCTTT (TAP1)	NP_000584.2:n.2220+48_2220+51delinsCTTT
NM_001292022.1:c.1437+48_1437+51delinsCTTT (TAP1)	NP_001278951.1:n.1437+48_1437+51delinsCTTT
NM_001292022.2:c.1437+48_1437+51delinsCTTT (TAP1)	NP_001278951.1:n.1437+48_1437+51delinsCTTT
NM_000593.6:c.2040+48_2040+51delinsCTTT (TAP1) MANE Select	NP_000584.3:n.2040+48_2040+51delinsCTTT