Canonical Allele Identifier: CA439974771
Community Standard Title: NM_025074.7(FRAS1):c.2631A>T (p.Ser877=)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78363963A>T , CM000666.2:g.78363963A>T GRCh38
NC_000004.11:g.79285117A>T , CM000666.1:g.79285117A>T GRCh37
NC_000004.10:g.79504141A>T NCBI36
NG_015812.1:g.311394A>T
NG_015812.2:g.311394A>T

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.2631A>T MANE Select NP_079350.5:p.Ser877=
ENST00000512123.4:c.2631A>T MANE Select ENSP00000422834.2:p.Ser877=
NM_001166133.1:c.2631A>T NP_001159605.1:p.Ser877=
NM_001166133.2:c.2631A>T NP_001159605.1:p.Ser877=
NM_025074.6:c.2631A>T NP_079350.5:p.Ser877=
ENST00000264899.10:c.845-80140A>T ENSP00000264899.7:n.845-80140A>T
ENST00000325942.10:c.2631A>T ENSP00000326330.6:p.Ser877=
ENST00000325942.11:c.2631A>T ENSP00000326330.6:p.Ser877=
ENST00000512123.3:c.2631A>T ENSP00000422834.2:p.Ser877=
ENST00000682513.1:c.2631A>T ENSP00000508201.1:p.Ser877=
ENST00000684159.1:c.2631A>T ENSP00000506875.1:p.Ser877=
XM_006714314.1:c.2631A>T XP_006714377.1:p.Ser877=
XM_006714316.1:c.2631A>T XP_006714379.1:p.Ser877=
XM_006714316.3:c.2631A>T XP_006714379.1:p.Ser877=
XM_011532270.1:c.330A>T XP_011530572.1:p.Ser110=