Canonical Allele Identifier: CA439979184
Community Standard Title: NM_025074.7(FRAS1):c.8844C>T (p.Ser2948=)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78488966C>T , CM000666.2:g.78488966C>T GRCh38
NC_000004.11:g.79410120C>T , CM000666.1:g.79410120C>T GRCh37
NC_000004.10:g.79629144C>T NCBI36
NG_015812.1:g.436397C>T
NG_015812.2:g.436397C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.8844C>T MANE Select NP_079350.5:p.Ser2948=
ENST00000512123.4:c.8844C>T MANE Select ENSP00000422834.2:p.Ser2948=
NM_025074.6:c.8844C>T NP_079350.5:p.Ser2948=
ENST00000512123.3:c.8844C>T ENSP00000422834.2:p.Ser2948=
ENST00000682513.1:c.8844C>T ENSP00000508201.1:p.Ser2948=
XM_006714314.1:c.8838C>T XP_006714377.1:p.Ser2946=
XM_006714316.1:c.8616C>T XP_006714379.1:p.Ser2872=
XM_006714316.3:c.8616C>T XP_006714379.1:p.Ser2872=
XM_011532270.1:c.6543C>T XP_011530572.1:p.Ser2181=
XM_011532271.1:c.3732C>T XP_011530573.1:p.Ser1244=