Canonical Allele Identifier: CA1865459525

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95101756_95101757delinsGA , CM000671.2:g.95101756_95101757delinsGA GRCh38
NC_000009.11:g.97864038_97864039delinsGA , CM000671.1:g.97864038_97864039delinsGA GRCh37
NC_000009.10:g.96903859_96903860delinsGA NCBI36
NG_011707.1:g.220953_220954delinsTC , LRG_497:g.220953_220954delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000710812.1:n.410+20976_410+20977delinsGA (AOPEP)
ENST00000696260.1:n.2442_2443delinsTC (FANCC)
ENST00000289081.8:c.1627_1628delinsTC (FANCC) MANE Select ENSP00000289081.3:p.Ser543=
ENST00000375305.6:c.1627_1628delinsTC (FANCC) ENSP00000364454.1:p.Ser543=
ENST00000649334.1:c.1772_1773delinsTC (FANCC) ENSP00000497735.1:n.1772_1773delinsTC
ENST00000289081.7:c.1627_1628delinsTC (FANCC) ENSP00000289081.3:p.Ser543=
ENST00000375305.5:c.1627_1628delinsTC (FANCC) ENSP00000364454.1:p.Ser543=
NM_000136.2:c.1627_1628delinsTC , LRG_497t1:c.1627_1628delinsTC (FANCC) NP_000127.2:p.Ser543=
NM_001243743.1:c.1627_1628delinsTC (FANCC) NP_001230672.1:p.Ser543=
XM_005251802.2:c.946_947delinsTC (FANCC) XP_005251859.1:p.Ser316=
XM_006717001.1:c.1462_1463delinsTC (FANCC) XP_006717064.1:p.Ser488=
XM_011518365.1:c.1627_1628delinsTC (FANCC) XP_011516667.1:p.Ser543=
XM_011518367.1:c.1171_1172delinsTC (FANCC) XP_011516669.1:p.Ser391=
XM_011519121.1:c.2319+20976_2319+20977delinsGA (AOPEP) XP_011517423.1:n.2319+20976_2319+20977delinsGA
XM_005251802.3:c.946_947delinsTC (FANCC) XP_005251859.1:p.Ser316=
XM_006717001.3:c.1462_1463delinsTC (FANCC) XP_006717064.1:p.Ser488=
XM_011518365.3:c.1627_1628delinsTC (FANCC) XP_011516667.1:p.Ser543=
XM_011518367.2:c.1171_1172delinsTC (FANCC) XP_011516669.1:p.Ser391=
XM_011519121.3:c.2319+20976_2319+20977delinsGA (AOPEP) XP_011517423.1:n.2319+20976_2319+20977delinsGA
XM_017014452.2:c.1171_1172delinsTC (FANCC) XP_016869941.1:p.Ser391=
XM_017014453.1:c.1171_1172delinsTC (FANCC) XP_016869942.1:p.Ser391=
XM_017014454.1:c.1006_1007delinsTC (FANCC) XP_016869943.1:p.Ser336=
XM_024447451.1:c.1627_1628delinsTC (FANCC) XP_024303219.1:p.Ser543=
NM_000136.3:c.1627_1628delinsTC (FANCC) MANE Select NP_000127.2:p.Ser543=
NM_001243743.2:c.1627_1628delinsTC (FANCC) NP_001230672.1:p.Ser543=