Canonical Allele Identifier: CA347880659
Gene: AFF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.99554731T>C , CM000664.2:g.99554731T>C GRCh38
NC_000002.11:g.100171193T>C , CM000664.1:g.100171193T>C GRCh37
NC_000002.10:g.99537625T>C NCBI36
NG_052835.1:g.592853A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001386135.1:c.3287A>G MANE Select NP_001373064.1:p.Asn1096Ser
ENST00000672756.2:c.3287A>G MANE Select ENSP00000500419.1:p.Asn1096Ser
NM_001025108.1:c.3362A>G NP_001020279.1:p.Asn1121Ser
NM_001025108.2:c.3362A>G NP_001020279.1:p.Asn1121Ser
NM_002285.2:c.3287A>G NP_002276.2:p.Asn1096Ser
NM_002285.3:c.3287A>G NP_002276.2:p.Asn1096Ser
ENST00000317233.8:c.3287A>G ENSP00000317421.4:p.Asn1096Ser
ENST00000409236.6:c.3287A>G ENSP00000387207.1:p.Asn1096Ser
ENST00000409579.5:c.3362A>G ENSP00000386834.1:p.Asn1121Ser
ENST00000445815.1:c.413A>G ENSP00000416685.1:p.Asn138Ser
ENST00000445815.2:c.1397A>G ENSP00000416685.2:p.Asn466Ser
ENST00000671937.1:c.1022A>G
XM_005263943.2:c.3287A>G XP_005264000.2:p.Asn1096Ser
XM_005263943.4:c.3287A>G XP_005264000.2:p.Asn1096Ser
XM_005263945.2:c.2294A>G XP_005264002.1:p.Asn765Ser
XM_005263945.4:c.2294A>G XP_005264002.1:p.Asn765Ser
XM_011511169.1:c.3359A>G XP_011509471.1:p.Asn1120Ser
XM_011511169.3:c.3746A>G XP_011509471.2:p.Asn1249Ser
XM_011511170.1:c.3518A>G XP_011509472.1:p.Asn1173Ser
XM_011511170.2:c.3518A>G XP_011509472.1:p.Asn1173Ser
XM_011511171.1:c.3362A>G XP_011509473.1:p.Asn1121Ser
XM_011511171.3:c.3749A>G XP_011509473.2:p.Asn1250Ser
XM_011511172.1:c.3314A>G XP_011509474.1:p.Asn1105Ser
XM_011511173.1:c.3362A>G XP_011509475.1:p.Asn1121Ser
XM_011511173.3:c.3362A>G XP_011509475.1:p.Asn1121Ser
XM_011511174.1:c.3362A>G XP_011509476.1:p.Asn1121Ser
XM_011511174.3:c.3362A>G XP_011509476.1:p.Asn1121Ser
XM_011511175.1:c.3287A>G XP_011509477.1:p.Asn1096Ser
XM_011511175.3:c.3287A>G XP_011509477.1:p.Asn1096Ser
XM_011511176.1:c.3287A>G XP_011509478.1:p.Asn1096Ser
XM_011511176.3:c.3287A>G XP_011509478.1:p.Asn1096Ser
XM_011511177.1:c.3287A>G XP_011509479.1:p.Asn1096Ser
XM_011511177.3:c.3287A>G XP_011509479.1:p.Asn1096Ser
XM_011511178.1:c.2204A>G XP_011509480.1:p.Asn735Ser
XM_011511178.3:c.2204A>G XP_011509480.1:p.Asn735Ser
XM_011511179.1:c.2201A>G XP_011509481.1:p.Asn734Ser
XM_011511179.3:c.2201A>G XP_011509481.1:p.Asn734Ser
XM_017004085.2:c.2291A>G XP_016859574.1:p.Asn764Ser
XM_017004086.2:c.2195A>G XP_016859575.1:p.Asn732Ser
XM_017004087.2:c.2192A>G XP_016859576.1:p.Asn731Ser
XM_024452883.1:c.3749A>G XP_024308651.1:p.Asn1250Ser