Canonical Allele Identifier: CA1470450579
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78264949T= , CM000666.2:g.78264949T= GRCh38
NC_000004.11:g.79186103T= , CM000666.1:g.79186103T= GRCh37
NC_000004.10:g.79405127T= NCBI36
NG_015812.1:g.212380T=
NG_015812.2:g.212380T=

Transcript Alleles

HGVS Amino-acid change
ENST00000325942.11:c.604-76T= ENSP00000326330.6:n.604-76T=
ENST00000502446.6:c.604-76T= ENSP00000423645.2:n.604-76T=
ENST00000508900.2:c.604-76T= ENSP00000423809.2:n.604-76T=
ENST00000682513.1:c.604-76T= ENSP00000508201.1:n.604-76T=
ENST00000683711.1:n.924-76T=
ENST00000684159.1:c.604-76T= ENSP00000506875.1:n.604-76T=
ENST00000512123.4:c.604-76T= MANE Select ENSP00000422834.2:n.604-76T=
ENST00000264899.10:c.604-76T= ENSP00000264899.7:n.604-76T=
ENST00000325942.10:c.604-76T= ENSP00000326330.6:n.604-76T=
ENST00000502446.5:c.390-76T=
ENST00000508900.1:c.131-76T=
ENST00000512123.3:c.604-76T= ENSP00000422834.2:n.604-76T=
NM_001166133.1:c.604-76T= NP_001159605.1:n.604-76T=
NM_025074.6:c.604-76T= NP_079350.5:n.604-76T=
XM_006714314.1:c.604-76T= XP_006714377.1:n.604-76T=
XM_006714316.1:c.604-76T= XP_006714379.1:n.604-76T=
XM_006714316.3:c.604-76T= XP_006714379.1:n.604-76T=
NM_025074.7:c.604-76T= MANE Select NP_079350.5:n.604-76T=
NM_001166133.2:c.604-76T= NP_001159605.1:n.604-76T=