Canonical Allele Identifier: CA1957607118
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625273_22625281delinsCCTTCCCCA , CM000673.2:g.22625273_22625281delinsCCTTCCCCA GRCh38
NC_000011.9:g.22646819_22646827delinsCCTTCCCCA , CM000673.1:g.22646819_22646827delinsCCTTCCCCA GRCh37
NC_000011.8:g.22603395_22603403delinsCCTTCCCCA NCBI36
NG_007425.1:g.5561_5569delinsTGGGGAAGG , LRG_527:g.5561_5569delinsTGGGGAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.530_538delinsTGGGGAAGG MANE Select ENSP00000330875.3:p.Val177=
ENST00000327470.4:c.530_538delinsTGGGGAAGG ENSP00000330875.3:p.Val177=
NM_022725.3:c.530_538delinsTGGGGAAGG , LRG_527t1:c.530_538delinsTGGGGAAGG NP_073562.1:p.Val177=
NM_022725.4:c.530_538delinsTGGGGAAGG MANE Select NP_073562.1:p.Val177=
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