Canonical Allele Identifier: CA2250421070
Community Standard Title: NM_144997.7(FLCN):c.708_709delinsCG (p.Asn236=)
Gene: FLCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17222571_17222572delinsCG , CM000679.2:g.17222571_17222572delinsCG GRCh38
NC_000017.10:g.17125885_17125886delinsCG , CM000679.1:g.17125885_17125886delinsCG GRCh37
NC_000017.9:g.17066610_17066611delinsCG NCBI36
NG_008001.2:g.19617_19618delinsCG , LRG_325:g.19617_19618delinsCG

Transcript Alleles

HGVS Amino-acid Change
NM_144997.7:c.708_709delinsCG MANE Select NP_659434.2:p.Asn236=
ENST00000285071.9:c.708_709delinsCG MANE Select ENSP00000285071.4:p.Asn236=
NM_001353229.1:c.762_763delinsCG NP_001340158.1:p.Asn254=
NM_001353229.2:c.762_763delinsCG NP_001340158.1:p.Asn254=
NM_001353230.1:c.708_709delinsCG NP_001340159.1:p.Asn236=
NM_001353230.2:c.708_709delinsCG NP_001340159.1:p.Asn236=
NM_001353231.1:c.708_709delinsCG NP_001340160.1:p.Asn236=
NM_001353231.2:c.708_709delinsCG NP_001340160.1:p.Asn236=
NM_144606.5:c.708_709delinsCG NP_653207.1:p.Asn236=
NM_144606.6:c.708_709delinsCG NP_653207.1:p.Asn236=
NM_144606.7:c.708_709delinsCG NP_653207.1:p.Asn236=
NM_144997.5:c.708_709delinsCG , LRG_325t1:c.708_709delinsCG NP_659434.2:p.Asn236=
NM_144997.6:c.708_709delinsCG NP_659434.2:p.Asn236=
ENST00000285071.8:c.708_709delinsCG ENSP00000285071.4:p.Asn236=
ENST00000389169.9:c.708_709delinsCG ENSP00000373821.5:p.Asn236=
ENST00000427497.3:c.149-3518_149-3517delinsCG ENSP00000394249.3:n.149-3518_149-3517delinsCG
ENST00000466317.1:n.551_552delinsCG
ENST00000480316.1:n.674_675delinsCG
XM_011523714.1:c.762_763delinsCG XP_011522016.1:p.Asn254=
XM_011523714.3:c.762_763delinsCG XP_011522016.1:p.Asn254=
XM_011523715.1:c.762_763delinsCG XP_011522017.1:p.Asn254=
XM_011523716.1:c.762_763delinsCG XP_011522018.1:p.Asn254=
XM_011523717.1:c.762_763delinsCG XP_011522019.1:p.Asn254=
XM_011523718.1:c.762_763delinsCG XP_011522020.1:p.Asn254=
XM_011523718.3:c.762_763delinsCG XP_011522020.1:p.Asn254=
XM_011523719.1:c.762_763delinsCG XP_011522021.1:p.Asn254=
XM_011523719.3:c.762_763delinsCG XP_011522021.1:p.Asn254=
XM_011523720.1:c.486_487delinsCG XP_011522022.1:p.Asn162=
XM_011523721.1:c.762_763delinsCG XP_011522023.1:p.Asn254=
XM_011523721.3:c.762_763delinsCG XP_011522023.1:p.Asn254=
XM_017024305.2:c.762_763delinsCG XP_016879794.1:p.Asn254=
XM_017024308.1:c.708_709delinsCG XP_016879797.1:p.Asn236=
XM_017024309.2:c.486_487delinsCG XP_016879798.1:p.Asn162=
XM_024450635.1:c.762_763delinsCG XP_024306403.1:p.Asn254=
XR_001752445.2:n.1266_1267delinsCG
XR_934007.1:n.2102_2103delinsCG