Canonical Allele Identifier: CA1470450755
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78265057_78265071delinsTTGCCCGCAGTGCTC , CM000666.2:g.78265057_78265071delinsTTGCCCGCAGTGCTC GRCh38
NC_000004.11:g.79186211_79186225delinsTTGCCCGCAGTGCTC , CM000666.1:g.79186211_79186225delinsTTGCCCGCAGTGCTC GRCh37
NC_000004.10:g.79405235_79405249delinsTTGCCCGCAGTGCTC NCBI36
NG_015812.1:g.212488_212502delinsTTGCCCGCAGTGCTC
NG_015812.2:g.212488_212502delinsTTGCCCGCAGTGCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000325942.11:c.636_650delinsTTGCCCGCAGTGCTC ENSP00000326330.6:p.Cys212=
ENST00000502446.6:c.636_650delinsTTGCCCGCAGTGCTC ENSP00000423645.2:p.Cys212=
ENST00000508900.2:c.636_650delinsTTGCCCGCAGTGCTC ENSP00000423809.2:p.Cys212=
ENST00000682513.1:c.636_650delinsTTGCCCGCAGTGCTC ENSP00000508201.1:p.Cys212=
ENST00000683711.1:n.956_970delinsTTGCCCGCAGTGCTC
ENST00000684159.1:c.636_650delinsTTGCCCGCAGTGCTC ENSP00000506875.1:p.Cys212=
ENST00000512123.4:c.636_650delinsTTGCCCGCAGTGCTC MANE Select ENSP00000422834.2:p.Cys212=
ENST00000264899.10:c.636_650delinsTTGCCCGCAGTGCTC ENSP00000264899.7:p.Cys212=
ENST00000325942.10:c.636_650delinsTTGCCCGCAGTGCTC ENSP00000326330.6:p.Cys212=
ENST00000502446.5:c.422_436delinsTTGCCCGCAGTGCTC
ENST00000508900.1:c.163_177delinsTTGCCCGCAGTGCTC
ENST00000512123.3:c.636_650delinsTTGCCCGCAGTGCTC ENSP00000422834.2:p.Cys212=
NM_001166133.1:c.636_650delinsTTGCCCGCAGTGCTC NP_001159605.1:p.Cys212=
NM_025074.6:c.636_650delinsTTGCCCGCAGTGCTC NP_079350.5:p.Cys212=
XM_006714314.1:c.636_650delinsTTGCCCGCAGTGCTC XP_006714377.1:p.Cys212=
XM_006714316.1:c.636_650delinsTTGCCCGCAGTGCTC XP_006714379.1:p.Cys212=
XM_006714316.3:c.636_650delinsTTGCCCGCAGTGCTC XP_006714379.1:p.Cys212=
NM_025074.7:c.636_650delinsTTGCCCGCAGTGCTC MANE Select NP_079350.5:p.Cys212=
NM_001166133.2:c.636_650delinsTTGCCCGCAGTGCTC NP_001159605.1:p.Cys212=