Canonical Allele Identifier: CA2190340896
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80177508_80177537delinsTTCATCAATATTGCTTTTCTTTCCAACAGG , CM000677.2:g.80177508_80177537delinsTTCATCAATATTGCTTTTCTTTCCAACAGG GRCh38
NC_000015.9:g.80469850_80469879delinsTTCATCAATATTGCTTTTCTTTCCAACAGG , CM000677.1:g.80469850_80469879delinsTTCATCAATATTGCTTTTCTTTCCAACAGG GRCh37
NC_000015.8:g.78256905_78256934delinsTTCATCAATATTGCTTTTCTTTCCAACAGG NCBI36
NG_012833.1:g.29510_29539delinsTTCATCAATATTGCTTTTCTTTCCAACAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682012.1:n.1003-29_1003delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
ENST00000561421.6:c.914-29_914delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
ENST00000646551.1:n.2528-29_2528delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
ENST00000261755.9:c.914-29_914delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
ENST00000407106.5:c.914-29_914delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
ENST00000539156.5:c.704-29_704delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
ENST00000559217.1:n.102_131delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
ENST00000561353.2:c.12-29_12delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
ENST00000561421.5:c.914-29_914delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
NM_000137.2:c.914-29_914delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
XM_024449872.1:c.914-29_914delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
NM_000137.4:c.914-29_914delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
NM_001374377.1:c.914-29_914delinsTTCATCAATATTGCTTTTCTTTCCAACAGG
NM_001374380.1:c.914-29_914delinsTTCATCAATATTGCTTTTCTTTCCAACAGG