Canonical Allele Identifier: CA2978525
Community Standard Title: NM_025074.7(FRAS1):c.8940A>G (p.Thr2980=)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78489062A>G , CM000666.2:g.78489062A>G GRCh38
NC_000004.11:g.79410216A>G , CM000666.1:g.79410216A>G GRCh37
NC_000004.10:g.79629240A>G NCBI36
NG_015812.1:g.436493A>G
NG_015812.2:g.436493A>G

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.8940A>G MANE Select NP_079350.5:p.Thr2980=
ENST00000512123.4:c.8940A>G MANE Select ENSP00000422834.2:p.Thr2980=
NM_025074.6:c.8940A>G NP_079350.5:p.Thr2980=
ENST00000512123.3:c.8940A>G ENSP00000422834.2:p.Thr2980=
ENST00000682513.1:c.8940A>G ENSP00000508201.1:p.Thr2980=
XM_006714314.1:c.8934A>G XP_006714377.1:p.Thr2978=
XM_006714316.1:c.8712A>G XP_006714379.1:p.Thr2904=
XM_006714316.3:c.8712A>G XP_006714379.1:p.Thr2904=
XM_011532270.1:c.6639A>G XP_011530572.1:p.Thr2213=
XM_011532271.1:c.3828A>G XP_011530573.1:p.Thr1276=