Canonical Allele Identifier: CA2770555465

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32848577_32848578insTCCTTTTCTTCCT , CM000668.2:g.32848577_32848578insTCCTTTTCTTCCT GRCh38
NC_000006.11:g.32816354_32816355insTCCTTTTCTTCCT , CM000668.1:g.32816354_32816355insTCCTTTTCTTCCT GRCh37
NC_000006.10:g.32924332_32924333insTCCTTTTCTTCCT NCBI36
NG_011759.1:g.10396_10397insGAAGAAAAGGAAG
NG_028165.1:g.1360_1361insGAAGAAAAGGAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000698420.1:c.*718+76_*718+77insGAAGAAAAGGAAG (TAP1) ENSP00000513708.1:n.*718+76_*718+77insGAAGAAAAGGAAG
ENST00000698421.1:c.*460+76_*460+77insGAAGAAAAGGAAG (TAP1) ENSP00000513709.1:n.*460+76_*460+77insGAAGAAAAGGAAG
ENST00000698422.1:c.1377+414_1377+415insGAAGAAAAGGAAG (TAP1) ENSP00000513710.1:n.1377+414_1377+415insGAAGAAAAGGAAG
ENST00000698423.1:c.1566+76_1566+77insGAAGAAAAGGAAG (TAP1) ENSP00000513711.1:n.1566+76_1566+77insGAAGAAAAGGAAG
ENST00000698424.1:c.1437+76_1437+77insGAAGAAAAGGAAG (TAP1) ENSP00000513712.1:n.1437+76_1437+77insGAAGAAAAGGAAG
ENST00000354258.5:c.1566+76_1566+77insGAAGAAAAGGAAG (TAP1) MANE Select ENSP00000346206.5:n.1566+76_1566+77insGAAGAAAAGGAAG
ENST00000643049.2:c.142-514_142-513insGAAGAAAAGGAAG (TAP1) ENSP00000494148.2:n.142-514_142-513insGAAGAAAAGGAAG
ENST00000643923.1:n.1002+76_1002+77insGAAGAAAAGGAAG (TAP1)
ENST00000645078.1:n.1161+76_1161+77insGAAGAAAAGGAAG (TAP1)
ENST00000354258.4:c.1746+76_1746+77insGAAGAAAAGGAAG (TAP1) ENSP00000346206.4:n.1746+76_1746+77insGAAGAAAAGGAAG
ENST00000395330.5:c.-10+4303_-10+4304insTCCTTTTCTTCCT (PSMB9) ENSP00000378739.1:n.-10+4303_-10+4304insTCCTTTTCTTCCT
ENST00000414474.5:c.-10+3707_-10+3708insTCCTTTTCTTCCT (PSMB9) ENSP00000394363.1:n.-10+3707_-10+3708insTCCTTTTCTTCCT
ENST00000486332.1:n.1491+76_1491+77insGAAGAAAAGGAAG (TAP1)
NM_000593.5:c.1746+76_1746+77insGAAGAAAAGGAAG (TAP1) NP_000584.2:n.1746+76_1746+77insGAAGAAAAGGAAG
NM_001292022.1:c.963+76_963+77insGAAGAAAAGGAAG (TAP1) NP_001278951.1:n.963+76_963+77insGAAGAAAAGGAAG
NM_001292022.2:c.963+76_963+77insGAAGAAAAGGAAG (TAP1) NP_001278951.1:n.963+76_963+77insGAAGAAAAGGAAG
NM_000593.6:c.1566+76_1566+77insGAAGAAAAGGAAG (TAP1) MANE Select NP_000584.3:n.1566+76_1566+77insGAAGAAAAGGAAG