Canonical Allele Identifier: CA357382310
Gene: FRAS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78511363A>C , CM000666.2:g.78511363A>C GRCh38
NC_000004.11:g.79432517A>C , CM000666.1:g.79432517A>C GRCh37
NC_000004.10:g.79651541A>C NCBI36
NG_015812.1:g.458794A>C
NG_015812.2:g.458794A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682513.1:c.9870A>C ENSP00000508201.1:p.Leu3290Phe
ENST00000512123.4:c.9870A>C MANE Select ENSP00000422834.2:p.Leu3290Phe
ENST00000512123.3:c.9870A>C ENSP00000422834.2:p.Leu3290Phe
NM_025074.6:c.9870A>C NP_079350.5:p.Leu3290Phe
XM_006714314.1:c.9864A>C XP_006714377.1:p.Leu3288Phe
XM_006714316.1:c.9642A>C XP_006714379.1:p.Leu3214Phe
XM_011532270.1:c.7569A>C XP_011530572.1:p.Leu2523Phe
XM_011532271.1:c.4758A>C XP_011530573.1:p.Leu1586Phe
XM_006714316.3:c.9642A>C XP_006714379.1:p.Leu3214Phe
NM_025074.7:c.9870A>C MANE Select NP_079350.5:p.Leu3290Phe