Canonical Allele Identifier: CA357398982
Community Standard Title: NM_025074.7(FRAS1):c.11158C>T (p.Gln3720Ter)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78537060C>T , CM000666.2:g.78537060C>T GRCh38
NC_000004.11:g.79458214C>T , CM000666.1:g.79458214C>T GRCh37
NC_000004.10:g.79677238C>T NCBI36
NG_015812.1:g.484491C>T
NG_015812.2:g.484491C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.11158C>T MANE Select NP_079350.5:p.Gln3720Ter
ENST00000512123.4:c.11158C>T MANE Select ENSP00000422834.2:p.Gln3720Ter
NM_025074.6:c.11158C>T NP_079350.5:p.Gln3720Ter
ENST00000512123.3:c.11158C>T ENSP00000422834.2:p.Gln3720Ter
XM_006714314.1:c.11152C>T XP_006714377.1:p.Gln3718Ter
XM_006714316.1:c.10930C>T XP_006714379.1:p.Gln3644Ter
XM_006714316.3:c.10930C>T XP_006714379.1:p.Gln3644Ter
XM_011532270.1:c.8857C>T XP_011530572.1:p.Gln2953Ter
XM_011532271.1:c.6046C>T XP_011530573.1:p.Gln2016Ter