Canonical Allele Identifier: CA2580068360
Community Standard Title: NM_001386135.1(AFF3):c.3351_3356dup (p.Ser1118_Pro1119dup)
Gene: AFF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.99554518_99554523dup , CM000664.2:g.99554518_99554523dup GRCh38
NC_000002.11:g.100170980_100170985dup , CM000664.1:g.100170980_100170985dup GRCh37
NC_000002.10:g.99537412_99537417dup NCBI36
NG_052835.1:g.593065_593070dup

Transcript Alleles

HGVS Amino-acid Change
NM_001386135.1:c.3351_3356dup MANE Select NP_001373064.1:p.Pro1119_Met1120insSerPro
ENST00000672756.2:c.3351_3356dup MANE Select ENSP00000500419.1:p.Pro1119_Met1120insSerPro
NM_001025108.1:c.3426_3431dup NP_001020279.1:p.Pro1144_Met1145insSerPro
NM_001025108.2:c.3426_3431dup NP_001020279.1:p.Pro1144_Met1145insSerPro
NM_002285.2:c.3351_3356dup NP_002276.2:p.Pro1119_Met1120insSerPro
NM_002285.3:c.3351_3356dup NP_002276.2:p.Pro1119_Met1120insSerPro
ENST00000317233.8:c.3351_3356dup ENSP00000317421.4:p.Pro1119_Met1120insSerPro
ENST00000409236.6:c.3351_3356dup ENSP00000387207.1:p.Pro1119_Met1120insSerPro
ENST00000409579.5:c.3426_3431dup ENSP00000386834.1:p.Pro1144_Met1145insSerPro
ENST00000445815.1:c.462-33_462-28dup ENSP00000416685.1:n.462-33_462-28dup
ENST00000445815.2:c.1446-33_1446-28dup ENSP00000416685.2:n.1446-33_1446-28dup
ENST00000671937.1:c.1071-33_1071-28dup
XM_005263943.2:c.3351_3356dup XP_005264000.2:p.Pro1119_Met1120insSerPro
XM_005263943.4:c.3351_3356dup XP_005264000.2:p.Pro1119_Met1120insSerPro
XM_005263945.2:c.2358_2363dup XP_005264002.1:p.Pro788_Met789insSerPro
XM_005263945.4:c.2358_2363dup XP_005264002.1:p.Pro788_Met789insSerPro
XM_011511169.1:c.3423_3428dup XP_011509471.1:p.Pro1143_Met1144insSerPro
XM_011511169.3:c.3810_3815dup XP_011509471.2:p.Pro1272_Met1273insSerPro
XM_011511170.1:c.3582_3587dup XP_011509472.1:p.Pro1196_Met1197insSerPro
XM_011511170.2:c.3582_3587dup XP_011509472.1:p.Pro1196_Met1197insSerPro
XM_011511171.1:c.3411-33_3411-28dup XP_011509473.1:n.3411-33_3411-28dup
XM_011511171.3:c.3798-33_3798-28dup XP_011509473.2:n.3798-33_3798-28dup
XM_011511172.1:c.3378_3383dup XP_011509474.1:p.Pro1128_Met1129insSerPro
XM_011511173.1:c.3426_3431dup XP_011509475.1:p.Pro1144_Met1145insSerPro
XM_011511173.3:c.3426_3431dup XP_011509475.1:p.Pro1144_Met1145insSerPro
XM_011511174.1:c.3426_3431dup XP_011509476.1:p.Pro1144_Met1145insSerPro
XM_011511174.3:c.3426_3431dup XP_011509476.1:p.Pro1144_Met1145insSerPro
XM_011511175.1:c.3351_3356dup XP_011509477.1:p.Pro1119_Met1120insSerPro
XM_011511175.3:c.3351_3356dup XP_011509477.1:p.Pro1119_Met1120insSerPro
XM_011511176.1:c.3351_3356dup XP_011509478.1:p.Pro1119_Met1120insSerPro
XM_011511176.3:c.3351_3356dup XP_011509478.1:p.Pro1119_Met1120insSerPro
XM_011511177.1:c.3351_3356dup XP_011509479.1:p.Pro1119_Met1120insSerPro
XM_011511177.3:c.3351_3356dup XP_011509479.1:p.Pro1119_Met1120insSerPro
XM_011511178.1:c.2268_2273dup XP_011509480.1:p.Pro758_Met759insSerPro
XM_011511178.3:c.2268_2273dup XP_011509480.1:p.Pro758_Met759insSerPro
XM_011511179.1:c.2265_2270dup XP_011509481.1:p.Pro757_Met758insSerPro
XM_011511179.3:c.2265_2270dup XP_011509481.1:p.Pro757_Met758insSerPro
XM_017004085.2:c.2355_2360dup XP_016859574.1:p.Pro787_Met788insSerPro
XM_017004086.2:c.2259_2264dup XP_016859575.1:p.Pro755_Met756insSerPro
XM_017004087.2:c.2256_2261dup XP_016859576.1:p.Pro754_Met755insSerPro
XM_024452883.1:c.3813_3818dup XP_024308651.1:p.Pro1273_Met1274insSerPro