Canonical Allele Identifier: CA1670888

Gene: FANCL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.58241353G>C , CM000664.2:g.58241353G>C	GRCh38
NC_000002.11:g.58468488G>C , CM000664.1:g.58468488G>C	GRCh37
NC_000002.10:g.58321992G>C	NCBI36
NG_007418.1:g.5027C>G , LRG_501:g.5027C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402135.8:c.-40C>G	ENSP00000385021.3:n.-40C>G
ENST00000403676.6:c.-40C>G	ENSP00000384046.2:n.-40C>G
ENST00000449070.6:c.-40C>G	ENSP00000401280.2:n.-40C>G
ENST00000470506.2:n.20C>G
ENST00000696305.1:c.-40C>G	ENSP00000512543.1:n.-40C>G
ENST00000696306.1:c.-40C>G	ENSP00000512544.1:n.-40C>G
ENST00000696319.1:c.-40C>G	ENSP00000512557.1:n.-40C>G
ENST00000696326.1:c.-40C>G	ENSP00000512562.1:n.-40C>G
ENST00000696341.1:n.29C>G
ENST00000696373.1:c.-40C>G	ENSP00000512587.1:n.-40C>G
ENST00000696377.1:n.25C>G
ENST00000696379.1:c.-40C>G	ENSP00000512590.1:n.-40C>G
ENST00000696398.1:c.-40C>G	ENSP00000512604.1:n.-40C>G
ENST00000696399.1:n.12C>G
ENST00000696400.1:c.-40C>G	ENSP00000512605.1:n.-40C>G
ENST00000696411.1:n.29C>G
ENST00000696530.1:c.-40C>G	ENSP00000512692.1:n.-40C>G
ENST00000449070.5:c.-40C>G	ENSP00000401280.1:n.-40C>G
NM_001114636.1:c.-40C>G , LRG_501t1:c.-40C>G	NP_001108108.1:n.-40C>G
NM_018062.3:c.-40C>G , LRG_501t2:c.-40C>G	NP_060532.2:n.-40C>G
XM_005264395.2:c.-40C>G	XP_005264452.1:n.-40C>G
XM_011532939.1:c.-40C>G	XP_011531241.1:n.-40C>G
XM_011532940.1:c.-40C>G	XP_011531242.1:n.-40C>G
XM_011532941.1:c.-40C>G	XP_011531243.1:n.-40C>G
XM_011532942.1:c.-40C>G	XP_011531244.1:n.-40C>G
XM_011532943.1:c.219C>G	XP_011531245.1:p.Ser73Arg
XR_939692.1:n.28C>G
NR_156742.1:n.28C>G
XM_005264395.4:c.-40C>G	XP_005264452.1:n.-40C>G
XM_011532939.3:c.-40C>G	XP_011531241.1:n.-40C>G
XM_011532940.3:c.-40C>G	XP_011531242.1:n.-40C>G
XM_011532941.2:c.-40C>G	XP_011531243.1:n.-40C>G
XM_011532942.3:c.-40C>G	XP_011531244.1:n.-40C>G
XM_017004414.2:c.-40C>G	XP_016859903.1:n.-40C>G
XM_017004415.2:c.-40C>G	XP_016859904.1:n.-40C>G
XM_017004416.1:c.-113C>G	XP_016859905.1:n.-113C>G
XR_001738802.2:n.20C>G
XR_001738803.2:n.20C>G
XR_002959309.1:n.329C>G
XR_939692.2:n.20C>G