Canonical Allele Identifier: CA1031119725
Gene: FANCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.58241347A>G , CM000664.2:g.58241347A>G GRCh38
NC_000002.11:g.58468482A>G , CM000664.1:g.58468482A>G GRCh37
NC_000002.10:g.58321986A>G NCBI36
NG_007418.1:g.5033T>C , LRG_501:g.5033T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000402135.8:c.-34T>C ENSP00000385021.3:n.-34T>C
ENST00000403676.6:c.-34T>C ENSP00000384046.2:n.-34T>C
ENST00000417361.2:c.-34T>C ENSP00000389448.2:n.-34T>C
ENST00000449070.6:c.-34T>C ENSP00000401280.2:n.-34T>C
ENST00000470506.2:n.26T>C
ENST00000481670.3:c.-34T>C ENSP00000483263.2:n.-34T>C
ENST00000696305.1:c.-34T>C ENSP00000512543.1:n.-34T>C
ENST00000696306.1:c.-34T>C ENSP00000512544.1:n.-34T>C
ENST00000696319.1:c.-34T>C ENSP00000512557.1:n.-34T>C
ENST00000696325.1:n.6T>C
ENST00000696326.1:c.-34T>C ENSP00000512562.1:n.-34T>C
ENST00000696341.1:n.35T>C
ENST00000696342.1:c.-34T>C ENSP00000512569.1:n.-34T>C
ENST00000696373.1:c.-34T>C ENSP00000512587.1:n.-34T>C
ENST00000696377.1:n.31T>C
ENST00000696379.1:c.-34T>C ENSP00000512590.1:n.-34T>C
ENST00000696398.1:c.-34T>C ENSP00000512604.1:n.-34T>C
ENST00000696399.1:n.18T>C
ENST00000696400.1:c.-34T>C ENSP00000512605.1:n.-34T>C
ENST00000696411.1:n.35T>C
ENST00000696438.1:c.-34T>C ENSP00000512630.1:n.-34T>C
ENST00000696496.1:n.6T>C
ENST00000696510.1:c.-34T>C ENSP00000512676.1:n.-34T>C
ENST00000696530.1:c.-34T>C ENSP00000512692.1:n.-34T>C
ENST00000696551.1:c.-34T>C ENSP00000512711.1:n.-34T>C
ENST00000233741.8:c.-34T>C ENSP00000233741.4:n.-34T>C
ENST00000402135.7:c.-34T>C ENSP00000385021.3:n.-34T>C
ENST00000417361.1:c.-107T>C ENSP00000389448.1:n.-107T>C
ENST00000449070.5:c.-34T>C ENSP00000401280.1:n.-34T>C
NM_001114636.1:c.-34T>C , LRG_501t1:c.-34T>C NP_001108108.1:n.-34T>C
NM_018062.3:c.-34T>C , LRG_501t2:c.-34T>C NP_060532.2:n.-34T>C
XM_005264395.2:c.-34T>C XP_005264452.1:n.-34T>C
XM_011532939.1:c.-34T>C XP_011531241.1:n.-34T>C
XM_011532940.1:c.-34T>C XP_011531242.1:n.-34T>C
XM_011532941.1:c.-34T>C XP_011531243.1:n.-34T>C
XM_011532942.1:c.-34T>C XP_011531244.1:n.-34T>C
XM_011532943.1:c.225T>C XP_011531245.1:p.Ser75=
XM_011532945.1:c.-107T>C XP_011531247.1:n.-107T>C
XR_939692.1:n.34T>C
NR_156742.1:n.34T>C
XM_005264395.4:c.-34T>C XP_005264452.1:n.-34T>C
XM_011532939.3:c.-34T>C XP_011531241.1:n.-34T>C
XM_011532940.3:c.-34T>C XP_011531242.1:n.-34T>C
XM_011532941.2:c.-34T>C XP_011531243.1:n.-34T>C
XM_011532942.3:c.-34T>C XP_011531244.1:n.-34T>C
XM_011532945.2:c.-107T>C XP_011531247.1:n.-107T>C
XM_017004414.2:c.-34T>C XP_016859903.1:n.-34T>C
XM_017004415.2:c.-34T>C XP_016859904.1:n.-34T>C
XM_017004416.1:c.-107T>C XP_016859905.1:n.-107T>C
XR_001738802.2:n.26T>C
XR_001738803.2:n.26T>C
XR_002959309.1:n.335T>C
XR_939692.2:n.26T>C