Canonical Allele Identifier: CA357396533
Community Standard Title: NM_025074.7(FRAS1):c.10999C>T (p.Gln3667Ter)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78534522C>T , CM000666.2:g.78534522C>T GRCh38
NC_000004.11:g.79455676C>T , CM000666.1:g.79455676C>T GRCh37
NC_000004.10:g.79674700C>T NCBI36
NG_015812.1:g.481953C>T
NG_015812.2:g.481953C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.10999C>T MANE Select NP_079350.5:p.Gln3667Ter
ENST00000512123.4:c.10999C>T MANE Select ENSP00000422834.2:p.Gln3667Ter
NM_025074.6:c.10999C>T NP_079350.5:p.Gln3667Ter
ENST00000512123.3:c.10999C>T ENSP00000422834.2:p.Gln3667Ter
XM_006714314.1:c.10993C>T XP_006714377.1:p.Gln3665Ter
XM_006714316.1:c.10771C>T XP_006714379.1:p.Gln3591Ter
XM_006714316.3:c.10771C>T XP_006714379.1:p.Gln3591Ter
XM_011532270.1:c.8698C>T XP_011530572.1:p.Gln2900Ter
XM_011532271.1:c.5887C>T XP_011530573.1:p.Gln1963Ter